Baclofen
- Product NDC
- 50090-2109
- 11-digit product format
- 500902109
- Labeler code
- 50090
- Product ID
- 50090-2109_d9fc1007-b2da-40be-9fe3-db0db3b0660a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record