propranolol hydrochloride
- Product NDC
- 55700-121
- 11-digit product format
- 557000121
- Labeler code
- 55700
- Product ID
- 55700-121_6dcd3556-f602-46be-bc70-6cd02b1a911e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA078703
- Marketing category
- ANDA
- Marketing start
- 2013-03-11
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 160 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record