Propranolol hydrochloride
- Product NDC
- 68071-2424
- 11-digit product format
- 680712424
- Labeler code
- 68071
- Product ID
- 68071-2424_c3563092-d9e9-53c5-e053-2995a90a9eb9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA070322
- Marketing category
- ANDA
- Marketing start
- 2019-10-31
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 80 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2424 | PROPRANOLOL HYDROCHLORIDE TABLET [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC | 20210529_c35639e8-975d-e16b-e053-2995a90ace85.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2424-1 | 68071242401 | 100 TABLET in 1 BOTTLE (68071-2424-1) | 100 tablet | 2021-05-27 | 0000-00-00 | No | No | Current |