Carvedilol
- Product NDC
- 52343-029
- 11-digit product format
- 523430029
- Labeler code
- 52343
- Product ID
- 52343-029_4dc27fdb-d38a-4466-b77a-ebc50170cff9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ACETRIS HEALTH, LLC
- Application
- ANDA078332
- Marketing category
- ANDA
- Marketing start
- 2007-09-05
- Marketing end
- 2020-12-01
- Substance
- CARVEDILOL
- Active strength
- 25 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record