Propranolol Hydrochloride
- Product NDC
- 63629-2276
- 11-digit product format
- 636292276
- Labeler code
- 63629
- Product ID
- 63629-2276_7d746e96-adcf-4bba-887f-9f6825a27b05
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA070221
- Marketing category
- ANDA
- Marketing start
- 2010-06-21
- 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 |
|---|
| 63629-2276-1 | 63629227601 | 100 TABLET in 1 BOTTLE (63629-2276-1) | 100 tablet | 2010-06-21 | 0000-00-00 | No | No | Current |