Baclofen
- Product NDC
- 63629-6406
- 11-digit product format
- 636296406
- Labeler code
- 63629
- Product ID
- 63629-6406_a3f8c9e7-c4fe-4109-ab42-47797a16d0dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077068
- Marketing category
- ANDA
- Marketing start
- 2005-08-30
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| H789N3FKE8 | BACLOFEN | 1134-47-0 | BACLOFEN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6406-1 | 63629640601 | 120 TABLET in 1 BOTTLE (63629-6406-1) | 120 tablet | 2015-09-09 | 0000-00-00 | No | No | Current |
| 63629-6406-2 | 63629640602 | 30 TABLET in 1 BOTTLE (63629-6406-2) | 30 tablet | 2016-01-11 | 0000-00-00 | No | No | Current |
| 63629-6406-3 | 63629640603 | 60 TABLET in 1 BOTTLE (63629-6406-3) | 60 tablet | 2016-01-11 | 0000-00-00 | No | No | Current |
| 63629-6406-4 | 63629640604 | 28 TABLET in 1 BOTTLE (63629-6406-4) | 28 tablet | 2016-12-23 | 0000-00-00 | No | No | Current |
| 63629-6406-5 | 63629640605 | 56 TABLET in 1 BOTTLE (63629-6406-5) | 56 tablet | 2016-12-23 | 0000-00-00 | No | No | Current |