Propranolol Hydrochloride
- Product NDC
- 68071-2484
- 11-digit product format
- 680712484
- Labeler code
- 68071
- Product ID
- 68071-2484_c80a014b-64d5-833d-e053-2995a90a9d02
- 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
- 40 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2484-3 | Propranolol Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 68071-2484-9 | Propranolol Hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2484 | PROPRANOLOL HYDROCHLORIDE TABLET [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC, 2 package rows | 20210727_c80a014b-64d6-833d-e053-2995a90a9d02.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2484-3 | 68071248403 | 30 TABLET in 1 BOTTLE (68071-2484-3) | 30 tablet | 2021-07-26 | 0000-00-00 | No | No | Current |
| 68071-2484-9 | 68071248409 | 90 TABLET in 1 BOTTLE (68071-2484-9) | 90 tablet | 2021-07-26 | 0000-00-00 | No | No | Current |