NDC 68382-138 – Topiramate

Topiramate 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC68382-138

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078235
Marketed since
March 27, 2009
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (4)

Package NDCDescriptionSince
68382-138-01100 TABLET, FILM COATED in 1 BOTTLE (68382-138-01)Mar 27, 2009
68382-138-05500 TABLET, FILM COATED in 1 BOTTLE (68382-138-05)Mar 27, 2009
68382-138-1460 TABLET, FILM COATED in 1 BOTTLE (68382-138-14)Mar 27, 2009
68382-138-1690 TABLET, FILM COATED in 1 BOTTLE (68382-138-16)Mar 27, 2009

Recalls mentioning this NDC

Other Topiramate products