Atenolol
- Product NDC
- 67296-1589
- 11-digit product format
- 672961589
- Labeler code
- 67296
- Product ID
- 67296-1589_d61c28e6-9c52-12db-e053-2a95a90a4e97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA076900
- Marketing category
- ANDA
- Marketing start
- 2018-01-01
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 25 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
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 |
|---|
| 67296-1589-3 | Atenolol | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1589 | ATENOLOL TABLET [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20220122_6a11aa30-15b0-3831-e053-2991aa0aba96.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 |
|---|
| 67296-1589-3 | 67296158903 | 30 TABLET in 1 BOTTLE (67296-1589-3) | 30 tablet | 2018-01-01 | 0000-00-00 | No | No | Current |