Baclofen
- Product NDC
- 63739-007
- 11-digit product format
- 637390007
- Labeler code
- 63739
- Product ID
- 63739-007_415f6680-3fef-4d02-b231-37d4b1f3c365
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation
- Application
- ANDA078220
- Marketing category
- ANDA
- Marketing start
- 2007-07-01
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record