Propranolol Hydrochloride
- Product NDC
- 71335-1140
- 11-digit product format
- 713351140
- Labeler code
- 71335
- Product ID
- 71335-1140_e7fc5ea2-8256-4a50-abe7-d40ce38b5011
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA070175
- Marketing category
- ANDA
- Marketing start
- 2016-09-19
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 71335-1140-1 | 71335114001 | 30 TABLET in 1 BOTTLE (71335-1140-1) | 30 tablet | 2019-03-13 | 0000-00-00 | No | No | Current |
| 71335-1140-2 | 71335114002 | 60 TABLET in 1 BOTTLE (71335-1140-2) | 60 tablet | 2019-03-13 | 0000-00-00 | No | No | Current |
| 71335-1140-3 | 71335114003 | 100 TABLET in 1 BOTTLE (71335-1140-3) | 100 tablet | 2019-03-13 | 0000-00-00 | No | No | Current |
| 71335-1140-4 | 71335114004 | 90 TABLET in 1 BOTTLE (71335-1140-4) | 90 tablet | 2019-03-13 | 0000-00-00 | No | No | Current |