71335-1041 : Gabapentin 800 mg Oral Tablet, Film Coated

NDC:	71335-1041
Labeler:	Bryant Ranch Prepack
Product Type:	Human Prescription Drug
Drug Name:	Gabapentin
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA203244
Rev. Date:	Jan 11, 2014

Appearance:

Markings:	NT;151
Shapes:	Oval
Colors:	White
Size (mm):	10
Segments: ^*	2
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

NDC Package Codes:

71335-1041-1: 90 TABLET, FILM COATED IN 1 BOTTLE (71335‑1041‑1)
71335-1041-2: 18 TABLET, FILM COATED IN 1 BOTTLE (71335‑1041‑2)
71335-1041-3: 58 TABLET, FILM COATED IN 1 BOTTLE (71335‑1041‑3)
71335-1041-4: 60 TABLET, FILM COATED IN 1 BOTTLE (71335‑1041‑4)
71335-1041-5: 30 TABLET, FILM COATED IN 1 BOTTLE (71335‑1041‑5)
71335-1041-6: 120 TABLET, FILM COATED IN 1 BOTTLE (71335‑1041‑6)

Active Ingredients:

Gabapentin

Dosage Strength:

800 mg

Inactive Ingredients:

Copovidone K25-31
Hydroxypropyl Cellulose, Unspecified
Magnesium Stearate
Mannitol
Poloxamer 407
Talc
Low-substituted Hydroxypropyl Cellulose, Unspecified
Polyvinyl Alcohol, Unspecified
Titanium Dioxide
Polyethylene Glycol, Unspecified /

Pharmaceutical Classes:

Anti-epileptic Agent [EPC]
Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC QR Code

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NDC 71335-1041 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.