NDC 29300-117 – Topiramate

Topiramate 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC29300-117

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090162
Marketed since
July 1, 2013
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (4)

Package NDCDescriptionSince
29300-117-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-117-01)Jul 1, 2013
29300-117-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-117-05)Jul 1, 2013
29300-117-101000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-117-10)Jul 1, 2013
29300-117-1660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-117-16)Jul 1, 2013

Recalls mentioning this NDC

Other Topiramate products