Propranolol Hydrochloride
- Product NDC
- 70934-922
- 11-digit product format
- 709340922
- Labeler code
- 70934
- Product ID
- 70934-922_dc661c83-f91e-351a-e053-2a95a90a6e8a
- 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
- 2021-11-12
- 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 |
|---|
| 70934-922-30 | 70934092230 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-922-30) | 30 tablet | 2022-04-11 | 0000-00-00 | No | No | Current |
| 70934-922-90 | 70934092290 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-922-90) | 90 tablet | 2021-11-12 | 0000-00-00 | No | No | Current |