Propranolol Hydrochloride
- Product NDC
- 50268-701
- 11-digit product format
- 502680701
- Labeler code
- 50268
- Product ID
- 50268-701_d5dfb02c-43dd-2099-e053-2995a90a8afb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA070176
- Marketing category
- ANDA
- Marketing start
- 2018-01-15
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 20 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 |
|---|
| 50268-701-15 | 50268070115 | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-701-15) > 1 TABLET in 1 BLISTER PACK (50268-701-11) | 50 blister pack | 2018-01-15 | 0000-00-00 | No | No | Current |