Baclofen
- Product NDC
- 68071-4905
- 11-digit product format
- 680714905
- Labeler code
- 68071
- Product ID
- 68071-4905_bb9ef3ab-87be-6a65-e053-2a95a90a0c5b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA072235
- Marketing category
- ANDA
- Marketing start
- 1988-07-21
- 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
- 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 |
|---|
| 68071-4905-3 | 68071490503 | 30 TABLET in 1 BOTTLE (68071-4905-3) | 30 tablet | 2019-05-22 | 0000-00-00 | No | No | Current |