Topiramate
- Product NDC
- 60429-772
- 11-digit product format
- 604290772
- Labeler code
- 60429
- Product ID
- 60429-772_be4e1a6e-ecdf-eb94-e053-2995a90a8a0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- topiramate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA079162
- Marketing category
- ANDA
- Marketing start
- 2011-07-08
- Marketing end
- 0000-00-00
- Substance
- TOPIRAMATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 3A4 Inducers [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-772-10 | 60429077210 | 1000 TABLET in 1 BOTTLE (60429-772-10) | 1000 tablet | 2011-07-08 | 0000-00-00 | No | No | Current |
| 60429-772-60 | 60429077260 | 60 TABLET in 1 BOTTLE (60429-772-60) | 60 tablet | 2011-07-08 | 0000-00-00 | No | No | Current |