CARVEDILOL
- Product NDC
- 69097-265
- 11-digit product format
- 690970265
- Labeler code
- 69097
- Product ID
- 69097-265_98a2a3d4-f553-4d39-916e-ececd0ef8eb4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- carvedilol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cipla USA Inc.
- Application
- ANDA077474
- Marketing category
- ANDA
- Marketing start
- 2007-09-05
- Marketing end
- 0000-00-00
- Substance
- CARVEDILOL
- Active strength
- 13 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record