Propranolol Hydrochloride
- Product NDC
- 70518-4454
- 11-digit product format
- 705184454
- Labeler code
- 70518
- Product ID
- 70518-4454_4d66ebae-c0c0-9798-e063-6294a90a72a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078955
- Marketing category
- ANDA
- Marketing start
- 2025-08-22
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Propranolol Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROPRANOLOL HYDROCHLORIDE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F8A3652H1V |
| Rxcui | 856457 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4454-0 | Propranolol Hydrochloride | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 3 |
| 70518-4454-1 | Propranolol Hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | | 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 |
|---|
| 70518-4454-0 | 70518445400 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-4454-0) | 30 tablet | 2025-08-22 | No | No | Current |
| 70518-4454-1 | 70518445401 | 30 TABLET in 1 BLISTER PACK (70518-4454-1) | 30 tablet | 2026-03-19 | No | No | Current |