Propranolol Hydrochloride
- Product NDC
- 71335-1120
- 11-digit product format
- 713351120
- Labeler code
- 71335
- Product ID
- 71335-1120_b8b2eb4c-b8fb-41c4-ba91-c23ba04cd0a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA070176
- Marketing category
- ANDA
- Marketing start
- 1986-05-13
- 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
- 2021-12-31
- 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 |
|---|
| 71335-1120-1 | 71335112001 | 20 TABLET in 1 BOTTLE (71335-1120-1) | 20 tablet | 2015-02-27 | 0000-00-00 | No | No | Current |
| 71335-1120-2 | 71335112002 | 30 TABLET in 1 BOTTLE (71335-1120-2) | 30 tablet | 2015-02-27 | 0000-00-00 | No | No | Current |
| 71335-1120-3 | 71335112003 | 100 TABLET in 1 BOTTLE (71335-1120-3) | 100 tablet | 2015-02-27 | 0000-00-00 | No | No | Current |
| 71335-1120-4 | 71335112004 | 60 TABLET in 1 BOTTLE (71335-1120-4) | 60 tablet | 2015-02-27 | 0000-00-00 | No | No | Current |
| 71335-1120-5 | 71335112005 | 90 TABLET in 1 BOTTLE (71335-1120-5) | 90 tablet | 2015-02-27 | 0000-00-00 | No | No | Current |
| 71335-1120-6 | 71335112006 | 180 TABLET in 1 BOTTLE (71335-1120-6) | 180 tablet | 2015-02-27 | 0000-00-00 | No | No | Current |
| 71335-1120-7 | 71335112007 | 28 TABLET in 1 BOTTLE (71335-1120-7) | 28 tablet | 2015-02-27 | 0000-00-00 | No | No | Current |