Propranolol Hydrochloride
- Product NDC
- 70518-1954
- 11-digit product format
- 705181954
- Labeler code
- 70518
- Product ID
- 70518-1954_840162f6-5a28-6c1d-e053-2991aa0aea35
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA070176
- Marketing category
- ANDA
- Marketing start
- 2019-03-13
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 20 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