Baclofen
- Product NDC
- 68788-6903
- 11-digit product format
- 687886903
- Labeler code
- 68788
- Product ID
- 68788-6903_3bfec32b-12d2-4899-b508-1e87ebb814d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA072235
- Marketing category
- ANDA
- Marketing start
- 2017-02-22
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record