Propranolol Hydrochloride
- Product NDC
- 68788-6761
- 11-digit product format
- 687886761
- Labeler code
- 68788
- Product ID
- 68788-6761_5a910e22-2f3c-4570-9874-6e8b14d21f10
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078955
- Marketing category
- ANDA
- Marketing start
- 2012-07-26
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record