Pregabalin
- Product NDC
- 0093-7623
- 11-digit product format
- 000937623
- Labeler code
- 0093
- Product ID
- 0093-7623_5aedcd0e-c075-428f-abed-0bdc222e3aae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA091219
- Marketing category
- ANDA
- Marketing start
- 2019-07-22
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 50 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record