ATENOLOL
- Product NDC
- 61919-257
- 11-digit product format
- 619190257
- Labeler code
- 61919
- Product ID
- 61919-257_9c5970fb-9b64-6e87-e053-2a95a90a6889
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATENOLOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA077877
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- 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
- 2021-12-31
- 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 |
|---|
| 61919-257-30 | ATENOLOL | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 61919-257-90 | ATENOLOL | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-257 | ATENOLOL TABLET [DIRECT RX] | 3 | Legacy NDC, 2 package rows | 20200118_32066d3f-dd94-4db6-943f-581a2f7104e7.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 |
|---|
| 61919-257-30 | 61919025730 | 30 TABLET in 1 BOTTLE (61919-257-30) | 30 tablet | 2015-01-01 | 0000-00-00 | No | No | Current |
| 61919-257-90 | 61919025790 | 90 TABLET in 1 BOTTLE (61919-257-90) | 90 tablet | 2015-01-01 | 0000-00-00 | No | No | Current |