Propranolol Hydrochloride
- Product NDC
- 71205-590
- 11-digit product format
- 712050590
- Labeler code
- 71205
- Product ID
- 71205-590_0af558f8-6356-45ee-a7fc-8728d7d65d76
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA070322
- Marketing category
- ANDA
- Marketing start
- 2019-10-31
- 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
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-590-30 | 71205059030 | 30 TABLET in 1 BOTTLE (71205-590-30) | 30 tablet | 2021-07-14 | No | No | Historical |
| 71205-590-60 | 71205059060 | 60 TABLET in 1 BOTTLE (71205-590-60) | 60 tablet | 2021-07-14 | No | No | Historical |
| 71205-590-90 | 71205059090 | 90 TABLET in 1 BOTTLE (71205-590-90) | 90 tablet | 2021-07-14 | No | No | Historical |