Pregabalin
- Product NDC
- 60505-3796
- 11-digit product format
- 605053796
- Labeler code
- 60505
- Product ID
- 60505-3796_aa1fe661-3f3b-f456-f1ce-6212f5267042
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- ApotexCorp
- Application
- ANDA211685
- Marketing category
- ANDA
- Marketing start
- 2022-06-20
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 100 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 60505-3796-9 | 60505379609 | 90 CAPSULE in 1 BOTTLE (60505-3796-9) | 90 capsule | 2022-06-20 | 0000-00-00 | No | No | Current |