propranolol hydrochloride
- Product NDC
- 63629-2070
- 11-digit product format
- 636292070
- Labeler code
- 63629
- Product ID
- 63629-2070_d2b77af3-f4da-441d-9eb5-ff1865ade1fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078703
- Marketing category
- ANDA
- Marketing start
- 2013-03-11
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| F8A3652H1V | PROPRANOLOL HYDROCHLORIDE | 318-98-9 | PROPRANOLOL HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-2070-1 | 63629207001 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2070-1) | 2021-01-28 | No | No | Historical |