Atenolol
- Product NDC
- 53217-181
- 11-digit product format
- 532170181
- Labeler code
- 53217
- Product ID
- 53217-181_8f3e0e4f-b5c4-4d09-8146-50b20da24371
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA076900
- Marketing category
- ANDA
- Marketing start
- 2005-10-08
- 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
- 2019-12-31
- 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 |
|---|
| 53217-181-00 | Atenolol | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 53217-181-60 | Atenolol | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 53217-181-90 | Atenolol | 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 |
|---|
| 53217-181 | ATENOLOL TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 3 package rows | 20170224_eeb03292-9faf-4a20-a512-57e8850fe0fc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-181-00 | 53217018100 | 100 in 1 BOTTLE | Historical |
| 53217-181-60 | 53217018160 | 60 in 1 BOTTLE | Historical |
| 53217-181-90 | 53217018190 | 90 in 1 BOTTLE | Historical |