Pregabalin
- Product NDC
- 71335-1740
- 11-digit product format
- 713351740
- Labeler code
- 71335
- Product ID
- 71335-1740_cad95632-2134-41f7-a2ea-de66f9f3a0cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pregabalin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207799
- Marketing category
- ANDA
- Marketing start
- 2019-07-21
- Substance
- PREGABALIN
- Active strength
- 100 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 | Sample | Exclude flag | Status |
|---|
| 71335-1740-1 | 71335174001 | 30 CAPSULE in 1 BOTTLE (71335-1740-1) | 30 capsule | 2021-02-11 | No | No | Historical |
| 71335-1740-2 | 71335174002 | 90 CAPSULE in 1 BOTTLE (71335-1740-2) | 90 capsule | 2020-12-03 | No | No | Historical |
| 71335-1740-3 | 71335174003 | 60 CAPSULE in 1 BOTTLE (71335-1740-3) | 60 capsule | 2021-02-09 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pregabalin | Bryant Ranch Prepack | 2024-09-06 | HUMAN PRESCRIPTION DRUG LABEL | 104 |