propranolol hydrochloride
- Product NDC
- 71335-2315
- 11-digit product format
- 713352315
- Labeler code
- 71335
- Product ID
- 71335-2315_d29ee62f-3e89-4501-b241-2f01003a79f5
- 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
- 80 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
Additional Listing Data
- Finished product
- Yes
- Brand name base
- propranolol hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| PROPRANOLOL HYDROCHLORIDE | 80 mg/1 |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | F8A3652H1V |
| Rxcui | 856569 |
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 |
|---|
| 71335-2315-1 | 71335231501 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2315-1) | 2023-11-30 | No | No | Current |