Propranolol Hydrochloride
- Product NDC
- 70518-0833
- 11-digit product format
- 705180833
- Labeler code
- 70518
- Product ID
- 70518-0833_e2709151-75c4-6d2a-e053-2a95a90a8039
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA070178
- Marketing category
- ANDA
- Marketing start
- 2017-11-09
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0833-0 | 70518083300 | 30 TABLET in 1 BLISTER PACK (70518-0833-0) | 30 tablet | 2017-11-09 | 0000-00-00 | No | No | Current |
| 70518-0833-2 | 70518083302 | 100 POUCH in 1 BOX (70518-0833-2) > 1 TABLET in 1 POUCH (70518-0833-1) | 100 pouch | 2019-05-21 | 0000-00-00 | No | No | Current |