propranolol hydrochloride
- Product NDC
- 70518-1463
- 11-digit product format
- 705181463
- Labeler code
- 70518
- Product ID
- 70518-1463_4900c8ab-3b55-e02c-e063-6394a90ace9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078703
- Marketing category
- ANDA
- Marketing start
- 2018-10-04
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 120 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 | 120 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F8A3652H1V |
| Rxcui | 856460 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-1463-0 | propranolol hydrochloride | 90 in 1 BOTTLE, PLASTIC | CAPSULE, EXTENDED RELEASE | 90 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1463 | PROPRANOLOL HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [REMEDYREPACK INC.] | 9 | Current NDC, Legacy NDC, 1 package rows | 20250223_e0241448-5727-4c68-ae2a-6f41cd962d7c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1463-0 | 70518146300 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1463-0) | 2018-10-04 | 0000-00-00 | No | No | Current |