Propranolol Hydrochloride
- Product NDC
- 71335-0387
- 11-digit product format
- 713350387
- Labeler code
- 71335
- Product ID
- 71335-0387_f61c4388-8a9f-409f-b3bf-756b03f9da25
- 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
- 2009-02-25
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- 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 |
|---|
| 71335-0387-1 | 71335038701 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0387-1) | 2014-07-22 | 0000-00-00 | No | No | Current |
| 71335-0387-2 | 71335038702 | 18 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0387-2) | 2014-07-22 | 0000-00-00 | No | No | Current |
| 71335-0387-3 | 71335038703 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0387-3) | 2014-07-22 | 0000-00-00 | No | No | Current |
| 71335-0387-4 | 71335038704 | 28 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0387-4) | 2014-07-22 | 0000-00-00 | No | No | Current |