Baclofen
- Product NDC
- 63629-6883
- 11-digit product format
- 636296883
- Labeler code
- 63629
- Product ID
- 63629-6883_46007fc3-77e2-4420-969c-329d529e636f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA072234
- Marketing category
- ANDA
- Marketing start
- 1988-07-21
- Marketing end
- 0000-00-00
- Substance
- BACLOFEN
- Active strength
- 10 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
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 |
|---|
| 63629-6883-1 | 63629688301 | 30 TABLET in 1 BOTTLE (63629-6883-1) | 30 tablet | 2016-01-14 | 0000-00-00 | No | No | Current |
| 63629-6883-2 | 63629688302 | 90 TABLET in 1 BOTTLE (63629-6883-2) | 90 tablet | 2016-01-14 | 0000-00-00 | No | No | Current |