Propranolol Hydrochloride
- Product NDC
- 64725-0110
- 11-digit product format
- 647250110
- Labeler code
- 64725
- Product ID
- 64725-0110_8cac22bb-9205-4c92-a5ae-912ac62e632a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA078955
- Marketing category
- ANDA
- Marketing start
- 2008-10-13
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64725-0110-1 | Propranolol Hydrochloride | 30 in 1 CONTAINER | TABLET | 30 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-0110 | PROPRANOLOL HYDROCHLORIDE TABLET [TYA PHARMACEUTICALS] | 4 | Legacy NDC, 1 package rows | 20141027_164d9c0a-9501-4088-a43a-377933557721.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64725-0110-1 | 64725011001 | 30 in 1 CONTAINER | Historical |