PREGABALIN
- Product NDC
- 70518-2290
- 11-digit product format
- 705182290
- Labeler code
- 70518
- Product ID
- 70518-2290_c7b8e39f-4f68-cdca-e053-2a95a90a32ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREGABALIN
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA210432
- Marketing category
- ANDA
- Marketing start
- 2019-08-30
- Marketing end
- 0000-00-00
- Substance
- PREGABALIN
- Active strength
- 225 mg/1
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2290-0 | 70518229000 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2290-0) | 90 capsule | 2019-08-30 | 0000-00-00 | No | No | Current |