Propranolol Hydrochloride
- Product NDC
- 50436-4314
- 11-digit product format
- 504364314
- Labeler code
- 50436
- Product ID
- 50436-4314_90e51e66-005f-472b-b003-4df2c9ed3755
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA078955
- Marketing category
- ANDA
- Marketing start
- 2008-10-13
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-4314-2 | Propranolol Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-4314 | PROPRANOLOL HYDROCHLORIDE TABLET [UNIT DOSE SERVICES] | 4 | Legacy NDC, 1 package rows | 20170316_16d3417d-9080-4fc8-99cb-beb904120565.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-4314-2 | 50436431402 | 60 in 1 BOTTLE | Historical |