Pregabalin
- Product NDC
- 55700-964
- 11-digit product format
- 557000964
- Labeler code
- 55700
- Product ID
- 55700-964_ba339486-3e99-428e-9b9d-935f85688c9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREGABALIN
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA208677
- Marketing category
- ANDA
- Marketing start
- 2022-03-10
- Marketing end
- 2027-06-30
- Substance
- PREGABALIN
- Active strength
- 200 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 55JG375S6M | PREGABALIN | 148553-50-8 | PREGABALIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-964-60 | 55700096460 | 60 CAPSULE in 1 BOTTLE (55700-964-60) | 60 capsule | 2022-03-10 | 2027-06-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pregabalin | Quality Care Products, LLC | 2024-12-19 | HUMAN PRESCRIPTION DRUG LABEL | 3 |