Propranolol Hydrochloride
- Product NDC
- 71205-760
- 11-digit product format
- 712050760
- Labeler code
- 71205
- Product ID
- 71205-760_968353ed-eb79-4f96-9569-3efb220fc388
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA078494
- Marketing category
- ANDA
- Marketing start
- 2007-08-10
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 60 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 |
|---|
| 71205-760-30 | 71205076030 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-760-30) | 2023-02-09 | No | No | Historical |
| 71205-760-60 | 71205076060 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-760-60) | 2023-02-09 | No | No | Historical |
| 71205-760-90 | 71205076090 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-760-90) | 2023-02-09 | No | No | Historical |