NDC 47335-712 – Topiramate

Topiramate 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC47335-712

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090278
Marketed since
December 15, 2014
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (6)

Package NDCDescriptionSince
47335-712-08100 TABLET, FILM COATED in 1 BOTTLE (47335-712-08)Dec 15, 2014
47335-712-13500 TABLET, FILM COATED in 1 BOTTLE (47335-712-13)Dec 15, 2014
47335-712-181000 TABLET, FILM COATED in 1 BOTTLE (47335-712-18)Dec 15, 2014
47335-712-8330 TABLET, FILM COATED in 1 BOTTLE (47335-712-83)Dec 15, 2014
47335-712-8660 TABLET, FILM COATED in 1 BOTTLE (47335-712-86)Dec 15, 2014
47335-712-88100 TABLET, FILM COATED in 1 BOTTLE (47335-712-88)Dec 15, 2014

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