Gabapentin (Page 8 of 8)

Gabapentin

Label ImageLabel Image

Gabapentin

Label ImageLabel Image

Gabapentin

Label ImageLabel Image
GABAPENTIN gabapentin capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-0896(NDC:67877-223)
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
STARCH, CORN
ANHYDROUS LACTOSE
TALC
GELATIN, UNSPECIFIED
SODIUM LAURYL SULFATE
TITANIUM DIOXIDE
FERRIC OXIDE YELLOW
Product Characteristics
Color YELLOW (yellow) Score no score
Shape CAPSULE (Capsule) Size 19mm
Flavor Imprint Code 215
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-0896-7 15 CAPSULE in 1 BOTTLE None
2 NDC:50090-0896-1 30 CAPSULE in 1 BOTTLE None
3 NDC:50090-0896-4 90 CAPSULE in 1 BOTTLE None
4 NDC:50090-0896-6 270 CAPSULE in 1 BOTTLE None
5 NDC:50090-0896-2 60 CAPSULE in 1 BOTTLE None
6 NDC:50090-0896-5 240 CAPSULE in 1 BOTTLE None
7 NDC:50090-0896-0 100 CAPSULE in 1 BOTTLE None
8 NDC:50090-0896-3 120 CAPSULE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090858 01/29/2011
GABAPENTIN gabapentin capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-2107(NDC:67877-224)
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
STARCH, CORN
ANHYDROUS LACTOSE
TALC
GELATIN, UNSPECIFIED
SODIUM LAURYL SULFATE
FERRIC OXIDE RED
TITANIUM DIOXIDE
FERRIC OXIDE YELLOW
Product Characteristics
Color ORANGE (orange) Score no score
Shape CAPSULE (Capsule) Size 21mm
Flavor Imprint Code 214
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-2107-1 30 CAPSULE in 1 BOTTLE None
2 NDC:50090-2107-2 60 CAPSULE in 1 BOTTLE None
3 NDC:50090-2107-0 90 CAPSULE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090858 01/29/2011
GABAPENTIN gabapentin capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-3200(NDC:67877-222)
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
STARCH, CORN
ANHYDROUS LACTOSE
TALC
GELATIN, UNSPECIFIED
SODIUM LAURYL SULFATE
TITANIUM DIOXIDE
Product Characteristics
Color WHITE (White) Score no score
Shape CAPSULE (Capsule) Size 14mm
Flavor Imprint Code 216
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-3200-2 90 CAPSULE in 1 BOTTLE None
2 NDC:50090-3200-0 30 CAPSULE in 1 BOTTLE None
3 NDC:50090-3200-1 100 CAPSULE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090858 01/29/2011
Labeler — A-S Medication Solutions (830016429)
Establishment
Name Address ID/FEI Operations
A-S Medication Solutions 830016429 RELABEL (50090-3200), RELABEL (50090-0896), REPACK (50090-0896), RELABEL (50090-2107), REPACK (50090-2107), REPACK (50090-3200)

Revised: 06/2022 A-S Medication Solutions

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 © 2022. All Rights Reserved.