Propranolol Hydrochloride
- Product NDC
- 70934-581
- 11-digit product format
- 709340581
- Labeler code
- 70934
- Product ID
- 70934-581_abab7306-22e8-a99c-e053-2995a90a75c4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA070322
- Marketing category
- ANDA
- Marketing start
- 2020-02-26
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-581-30 | 70934058130 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-581-30) | 30 tablet | 2020-02-26 | 0000-00-00 | No | No | Current |
| 70934-581-90 | 70934058190 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-581-90) | 90 tablet | 2020-04-01 | 0000-00-00 | No | No | Current |