Pregabalin Extended Release
- Product NDC
- 47781-381
- 11-digit product format
- 477810381
- Labeler code
- 47781
- Product ID
- 47781-381_f060e976-f0be-c832-cf7e-f4be47c70e06
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREGABALIN
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Alvogen Inc.
- Application
- ANDA211593
- Marketing category
- ANDA
- Marketing start
- 2021-04-14
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 330 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 47781-381-30 | 47781038130 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47781-381-30) | 2021-04-14 | 0000-00-00 | No | No | Current |