Propranolol hydrochloride
- Product NDC
- 70518-3141
- 11-digit product format
- 705183141
- Labeler code
- 70518
- Product ID
- 70518-3141_c675036b-e25a-902e-e053-2995a90a2f69
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA070322
- Marketing category
- ANDA
- Marketing start
- 2021-07-05
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 80 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-3141-0 | 70518314100 | 30 TABLET in 1 BLISTER PACK (70518-3141-0) | 30 tablet | 2021-07-05 | 0000-00-00 | No | No | Current |