Propranolol Hydrochloride
- Product NDC
- 53002-4561
- 11-digit product format
- 530024561
- Labeler code
- 53002
- Product ID
- 53002-4561_0da01d7a-35d0-4de1-860c-71baadb40b89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA070175
- Marketing category
- ANDA
- Marketing start
- 1986-05-13
- 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
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-4561-0 | 53002456100 | 100 TABLET in 1 BOTTLE (53002-4561-0) | 100 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |
| 53002-4561-1 | 53002456101 | 10 TABLET in 1 BOTTLE (53002-4561-1) | 10 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |
| 53002-4561-3 | 53002456103 | 30 TABLET in 1 BOTTLE (53002-4561-3) | 30 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |