Propranolol Hydrochloride
- Product NDC
- 68788-7311
- 11-digit product format
- 687887311
- Labeler code
- 68788
- Product ID
- 68788-7311_b734492f-c4e0-4754-b85a-b82b84420647
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA070176
- Marketing category
- ANDA
- Marketing start
- 2019-01-02
- 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 |
|---|
| 68788-7311-3 | 68788731103 | 100 TABLET in 1 BOTTLE, PLASTIC (68788-7311-3) | 100 tablet | 2019-01-02 | 0000-00-00 | No | No | Current |