NDC 65862-174 – Topiramate

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

Human Prescription Drug

Product NDC65862-174

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078462
Marketed since
March 27, 2009
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (3)

Package NDCDescriptionSince
65862-174-05500 TABLET, FILM COATED in 1 BOTTLE (65862-174-05)Apr 11, 2022
65862-174-6060 TABLET, FILM COATED in 1 BOTTLE (65862-174-60)Mar 27, 2009
65862-174-991000 TABLET, FILM COATED in 1 BOTTLE (65862-174-99)Apr 11, 2022

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