Gabapentin (Page 8 of 8)

Package/Label Display Panel

NDC 77771-177-90

Gabapentin

Tablets, USP

600 mg

PHARMACIST: Provide a Medication
Guide to each patient when dispensing
Gabapentin Tablets.

Rx only 90 Tablets

Radha Pharmaceuticals Inc.

Gabapentin Tablets, USP 600 mg -- 100 Tablets label
(click image for full-size original)

NDC 77771-177-05

Gabapentin

Tablets, USP

600 mg

PHARMACIST: Provide a Medication Guide to each patient when dispensing Gabapentin Tablets.

Rx only 500 Tablets

Radha Pharmaceuticals Inc.

Gabapentin Tablets, USP 600 mg -- 500 Tablets label
(click image for full-size original)

NDC 77771-178-90

Gabapentin

Tablets, USP

800 mg

PHARMACIST: Provide a Medication
Guide to each patient when dispensing
Gabapentin Tablets.

Rx only 90 Tablets

Radha Pharmaceuticals Inc.

Gabapentin Tablets, USP 800 mg -- 100 Tablets label
(click image for full-size original)

NDC 77771-178-05

Gabapentin

Tablets, USP

800 mg

PHARMACIST: Provide a Medication Guide to each patient when dispensing Gabapentin Tablets.

Rx only 500 Tablets

Radha Pharmaceuticals Inc.

Gabapentin Tablets, USP 800 mg -- 500 Tablets label
(click image for full-size original)
GABAPENTIN gabapentin tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:77771-177
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
MANNITOL
MAGNESIUM STEARATE
HYDROXYPROPYL CELLULOSE, UNSPECIFIED
TALC
COPOVIDONE K25-31
CROSPOVIDONE, UNSPECIFIED
SILICON DIOXIDE
HYPROMELLOSE, UNSPECIFIED
TITANIUM DIOXIDE
POLYETHYLENE GLYCOL, UNSPECIFIED
Product Characteristics
Color white (White to off-white) Score 2 pieces
Shape CAPSULE Size 18mm
Flavor Imprint Code SG;177
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:77771-177-90 90 TABLET in 1 BOTTLE None
2 NDC:77771-177-05 500 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA205101 11/03/2023
GABAPENTIN gabapentin tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:77771-178
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
MANNITOL
MAGNESIUM STEARATE
HYDROXYPROPYL CELLULOSE, UNSPECIFIED
TALC
COPOVIDONE K25-31
CROSPOVIDONE, UNSPECIFIED
SILICON DIOXIDE
HYPROMELLOSE, UNSPECIFIED
TITANIUM DIOXIDE
POLYETHYLENE GLYCOL, UNSPECIFIED
Product Characteristics
Color white (White to off-white) Score 2 pieces
Shape CAPSULE Size 19mm
Flavor Imprint Code SG;178
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:77771-178-90 90 TABLET in 1 BOTTLE None
2 NDC:77771-178-05 500 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA205101 11/03/2023
Labeler — Radha Pharmaceuticals, Inc. (117634222)
Establishment
Name Address ID/FEI Operations
ScieGen Pharmaceuticals, Inc. 079391286 manufacture (77771-177), manufacture (77771-178), analysis (77771-177), analysis (77771-178)

Revised: 11/2023 Radha Pharmaceuticals, Inc.

All MedLibrary.org resources are included in as near-original form as possible, meaning that the information from the original provider has been rendered here with only typographical or stylistic modifications and not with any substantive alterations of content, meaning or intent.

This site is provided for educational and informational purposes only, in accordance with our Terms of Use, and is not intended as a substitute for the advice of a medical doctor, nurse, nurse practitioner or other qualified health professional.

Privacy Policy | Copyright © 2024. All Rights Reserved.