Baclofen
- Product NDC
- 68071-3001
- 11-digit product format
- 680713001
- Labeler code
- 68071
- Product ID
- 68071-3001_bb122c6d-6b76-f77e-e053-2a95a90ac059
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA077241
- Marketing category
- ANDA
- Marketing start
- 2005-12-01
- 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 |
|---|
| 68071-3001-2 | 68071300102 | 20 TABLET in 1 BOTTLE (68071-3001-2) | 20 tablet | 2017-03-29 | 0000-00-00 | No | No | Current |
| 68071-3001-3 | 68071300103 | 30 TABLET in 1 BOTTLE (68071-3001-3) | 30 tablet | 2017-03-29 | 0000-00-00 | No | No | Current |
| 68071-3001-6 | 68071300106 | 60 TABLET in 1 BOTTLE (68071-3001-6) | 60 tablet | 2017-03-29 | 0000-00-00 | No | No | Current |
| 68071-3001-9 | 68071300109 | 90 TABLET in 1 BOTTLE (68071-3001-9) | 90 tablet | 2017-03-29 | 0000-00-00 | No | No | Current |