Propranolol Hydrochloride
- Product NDC
- 50090-7618
- 11-digit product format
- 500907618
- Labeler code
- 50090
- Product ID
- 50090-7618_cc40a50e-44b2-4146-9796-b390066072fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078955
- Marketing category
- ANDA
- Marketing start
- 2024-09-19
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 40 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
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7618-1 | Propranolol Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 2 |
| 50090-7618-6 | Propranolol Hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7618-1 | 50090761801 | 60 TABLET in 1 BOTTLE (50090-7618-1) | 60 tablet | 2025-08-01 | No | No | Historical |
| 50090-7618-6 | 50090761806 | 90 TABLET in 1 BOTTLE (50090-7618-6) | 90 tablet | 2025-08-01 | No | No | Historical |