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What kinds of Chemical Ingredients are Included in Gabapentin?

PRINCIPAL DISPLAY PANEL – 100 mg capsule bottle label

ALWAYS DISPENSE WITH MEDICATION GUIDE

NDC 59762-5026-1
100 Capsules
GREENSTONE® BRAND
Gabapentin  capsules 100 mg
Rx only

PRINCIPAL DISPLAY PANEL – 300 mg capsule bottle label

ALWAYS DISPENSE WITH
MEDICATION GUIDE

NDC 59762-5027-1
100 Capsules
GREENSTONE® BRAND
Gabapentin
capsules
300 mg
Rx only

PRINCIPAL DISPLAY PANEL – 400 mg capsule bottle label

ALWAYS DISPENSE WITH
MEDICATION GUIDE

NDC 59762-5028-1
100 Capsules
GREENSTONE® BRAND
Gabapentin
capsules
400 mg
Rx only

PRINCIPAL DISPLAY PANEL – 600 mg tablet bottle label

ALWAYS DISPENSE WITH
MEDICATION GUIDE

NDC 59762-5023-1
100 Tablets
GREENSTONE® BRAND
Gabapentin
tablets
600 mg
Rx only

PRINCIPAL DISPLAY PANEL – 800 mg tablet bottle label

ALWAYS DISPENSE WITH
MEDICATION GUIDE

NDC 59762-5024-1
100 Tablets
GREENSTONE® BRAND
Gabapentin
tablets
800 mg
Rx only

PRINCIPAL DISPLAY PANEL – 470 mL Bottle Label

ALWAYS DISPENSE WITH MEDICATION GUIDE

NDC 59762-5025-1
470 mL
GREENSTONE® BRAND
Gabapentin
oral solution
250 mg / 5 mL
Rx only

Gabapentin 
Gabapentin capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:59762-5026
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Gabapentin (Gabapentin) Gabapentin 100 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE
STARCH, CORN
TALC
GELATIN
TITANIUM DIOXIDE
FD&C BLUE NO. 2
Product Characteristics
Color WHITE Score no score
Shape CAPSULE Size 16mm
Flavor Imprint Code G;5026
Contains
Packaging
# Item Code Package Description
1 NDC:59762-5026-1 100 CAPSULE in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA AUTHORIZED GENERIC NDA020235 12/30/1993
Gabapentin 
Gabapentin capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:59762-5027
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Gabapentin (Gabapentin) Gabapentin 300 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE
STARCH, CORN
TALC
GELATIN
TITANIUM DIOXIDE
FERRIC OXIDE YELLOW
FD&C BLUE NO. 2
Product Characteristics
Color YELLOW Score no score
Shape CAPSULE Size 19mm
Flavor Imprint Code G;5027
Contains
Packaging
# Item Code Package Description
1 NDC:59762-5027-1 100 CAPSULE in 1 BOTTLE
2 NDC:59762-5027-2 500 CAPSULE in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA AUTHORIZED GENERIC NDA020235 12/30/1993
Gabapentin 
Gabapentin capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:59762-5028
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Gabapentin (Gabapentin) Gabapentin 400 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE
STARCH, CORN
TALC
GELATIN
FERRIC OXIDE RED
TITANIUM DIOXIDE
FERRIC OXIDE YELLOW
FD&C BLUE NO. 2
Product Characteristics
Color ORANGE Score no score
Shape CAPSULE Size 22mm
Flavor Imprint Code G;5028
Contains
Packaging
# Item Code Package Description
1 NDC:59762-5028-1 100 CAPSULE in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA AUTHORIZED GENERIC NDA020235 12/30/1993
Gabapentin 
Gabapentin tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:59762-5023
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Gabapentin (Gabapentin) Gabapentin 600 mg
Inactive Ingredients
Ingredient Name Strength
POLOXAMER 407
STARCH, CORN
MAGNESIUM STEARATE
HYDROXYPROPYL CELLULOSE (TYPE H)
TALC
CANDELILLA WAX
WATER
Product Characteristics
Color WHITE Score 2 pieces
Shape OVAL Size 18mm
Flavor Imprint Code G;21
Contains
Packaging
# Item Code Package Description
1 NDC:59762-5023-1 100 TABLET, FILM COATED in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA AUTHORIZED GENERIC NDA020882 10/09/1998
Gabapentin 
Gabapentin tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:59762-5024
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Gabapentin (Gabapentin) Gabapentin 800 mg
Inactive Ingredients
Ingredient Name Strength
POLOXAMER 407
STARCH, CORN
MAGNESIUM STEARATE
HYDROXYPROPYL CELLULOSE (TYPE H)
TALC
CANDELILLA WAX
WATER
Product Characteristics
Color WHITE Score 2 pieces
Shape OVAL Size 19mm
Flavor Imprint Code G;22
Contains
Packaging
# Item Code Package Description
1 NDC:59762-5024-1 100 TABLET, FILM COATED in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA AUTHORIZED GENERIC NDA020882 10/09/1998
Gabapentin 
Gabapentin suspension
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:59762-5025
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Gabapentin (Gabapentin) Gabapentin 250 mg  in 5 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
XYLITOL
WATER
Product Characteristics
Color Score
Shape Size
Flavor STRAWBERRY (cool strawberry anise) Imprint Code
Contains
Packaging
# Item Code Package Description
1 NDC:59762-5025-1 470 mL in 1 BOTTLE, GLASS
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA AUTHORIZED GENERIC NDA021129 03/29/2011
Labeler – Greenstone LLC (825560733)
Registrant – Pfizer Inc (113480771)
Establishment
Name Address ID/FEI Operations
Pfizer Ireland Pharmaceuticals 989811526 API MANUFACTURE(59762-5023, 59762-5024, 59762-5025, 59762-5026, 59762-5027, 59762-5028)
Establishment
Name Address ID/FEI Operations
Pfizer Asia Pacific PTE LTD 894677996 API MANUFACTURE(59762-5023, 59762-5024, 59762-5025, 59762-5026, 59762-5027, 59762-5028)
Establishment
Name Address ID/FEI Operations
Pfizer Pharmaceuticals LLC 829084552 MANUFACTURE(59762-5023, 59762-5024, 59762-5025, 59762-5026, 59762-5027, 59762-5028)
Establishment
Name Address ID/FEI Operations
Hikal Ltd. 918602129 API MANUFACTURE(59762-5023, 59762-5024, 59762-5025, 59762-5026, 59762-5027, 59762-5028)
Establishment
Name Address ID/FEI Operations
DPT Laboratories, Ltd. 832224526 MANUFACTURE(59762-5025, 59762-5024, 59762-5023, 59762-5028, 59762-5027, 59762-5026), PACK(59762-5025, 59762-5024, 59762-5023, 59762-5028, 59762-5027, 59762-5026)
Establishment
Name Address ID/FEI Operations
Johnson & Johnson Healthcare Products Division of McNEIL-PPC, Inc. 801375143 MANUFACTURE(59762-5025, 59762-5024, 59762-5023, 59762-5028, 59762-5027, 59762-5026), PACK(59762-5025, 59762-5024, 59762-5023, 59762-5028, 59762-5027, 59762-5026)
Establishment
Name Address ID/FEI Operations
Orchid Chemicals & Pharmaceuticals Limited 650288850 MANUFACTURE(59762-5025, 59762-5024, 59762-5023, 59762-5028, 59762-5027, 59762-5026)
Establishment
Name Address ID/FEI Operations
ZACH SYSTEM SPA 517259979 API MANUFACTURE(59762-5025, 59762-5024, 59762-5023, 59762-5028, 59762-5027, 59762-5026)
Establishment
Name Address ID/FEI Operations
Pharmacia and Upjohn Company 829076566 MANUFACTURE(59762-5025, 59762-5024, 59762-5023, 59762-5028, 59762-5027, 59762-5026)
Establishment
Name Address ID/FEI Operations
Emcure Pharmaceuticals Limited 862602830 MANUFACTURE(59762-5025, 59762-5024, 59762-5023, 59762-5028, 59762-5027, 59762-5026), PACK(59762-5025, 59762-5024, 59762-5023, 59762-5028, 59762-5027, 59762-5026)
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