Propranolol Hydrochloride
- Product NDC
- 0904-7467
- 11-digit product format
- 009047467
- Labeler code
- 0904
- Product ID
- 0904-7467_b9cee427-7372-4b05-9d11-b6d1371f8081
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA071972
- Marketing category
- ANDA
- Marketing start
- 2025-11-21
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 0904-7467-61 | Propranolol Hydrochloride | 1 in 1 BLISTER PACK | TABLET | 1 | | 3 |
| 0904-7467-61 | Propranolol Hydrochloride | 100 in 1 CARTON | TABLET | 100 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0904-7467-61 | 00904746761 | 100 BLISTER PACK in 1 CARTON (0904-7467-61) / 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2025-11-21 | No | No | Historical |