Atenolol
- Product NDC
- 67296-1732
- 11-digit product format
- 672961732
- Labeler code
- 67296
- Product ID
- 67296-1732_b8dfb557-f1e3-0a82-e053-2a95a90a210c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2019-11-01
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 50 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 |
|---|
| 67296-1732-3 | Atenolol | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1732 | ATENOLOL TABLET [REDPHARM DRUG, INC.] | 2 | Legacy NDC, 1 package rows | 20210115_97280ed9-e804-7c8d-e053-2a95a90af142.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 |
|---|
| 67296-1732-3 | 67296173203 | 30 TABLET in 1 BOTTLE (67296-1732-3) | 30 tablet | 2019-11-01 | 0000-00-00 | No | No | Current |