Topiramate
- Product NDC
- 68788-6435
- 11-digit product format
- 687886435
- Labeler code
- 68788
- Product ID
- 68788-6435_81370248-8c82-4a95-9c5c-e7628d8d7c48
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Topiramate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals
- Application
- ANDA079162
- Marketing category
- ANDA
- Marketing start
- 2016-07-11
- Marketing end
- 0000-00-00
- Substance
- TOPIRAMATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Decreased Centr
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record