Baclofen
- Product NDC
- 63629-1226
- 11-digit product format
- 636291226
- Labeler code
- 63629
- Product ID
- 63629-1226_2a483651-d9ef-4f5d-834b-bdf19be60cf3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212378
- Marketing category
- ANDA
- Marketing start
- 2020-10-14
- Marketing end
- 0000-00-00
- Substance
- BACLOFEN
- Active strength
- 20 mg/1
- Pharmacologic classes
- GABA A Agonists [MoA], GABA B Agonists [MoA], gamma-Aminobutyric Acid-ergic Agonist [EPC]
- 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 |
|---|
| 63629-1226-1 | 63629122601 | 500 TABLET in 1 BOTTLE (63629-1226-1) | 500 tablet | 2021-01-14 | 0000-00-00 | No | No | Current |