Baclofen
- Product NDC
- 70518-0547
- 11-digit product format
- 705180547
- Labeler code
- 70518
- Product ID
- 70518-0547_85abe91a-a23d-6ef8-e053-2991aa0a2f90
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA072234
- Marketing category
- ANDA
- Marketing start
- 2017-05-18
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record