Propranolol Hydrochloride
- Product NDC
- 63629-1968
- 11-digit product format
- 636291968
- Labeler code
- 63629
- Product ID
- 63629-1968_d45e4dda-6984-40a2-8ac1-73507a4726e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA018553
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-12-21
- Marketing end
- 2023-06-30
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1968-1 | 63629196801 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-1968-1) | 2021-01-14 | 0000-00-00 | No | No | Current |