Propranolol Hydrochloride
- Product NDC
- 68788-7350
- 11-digit product format
- 687887350
- Labeler code
- 68788
- Product ID
- 68788-7350_eadc2f9d-3b1d-4540-89fa-862719d63d0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA070177
- Marketing category
- ANDA
- Marketing start
- 2019-03-07
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 40 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 |
|---|
| 68788-7350-1 | 68788735001 | 100 TABLET in 1 BOTTLE, PLASTIC (68788-7350-1) | 100 tablet | 2019-03-07 | 0000-00-00 | No | No | Current |
| 68788-7350-3 | 68788735003 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-7350-3) | 30 tablet | 2019-03-07 | 0000-00-00 | No | No | Current |
| 68788-7350-6 | 68788735006 | 60 TABLET in 1 BOTTLE, PLASTIC (68788-7350-6) | 60 tablet | 2019-03-07 | 0000-00-00 | No | No | Current |
| 68788-7350-9 | 68788735009 | 90 TABLET in 1 BOTTLE, PLASTIC (68788-7350-9) | 90 tablet | 2019-03-07 | 0000-00-00 | No | No | Current |