Atenolol
- Product NDC
- 51655-928
- 11-digit product format
- 516550928
- Labeler code
- 51655
- Product ID
- 51655-928_497445b1-cc97-62bc-e063-6394a90a8b45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA078512
- Marketing category
- ANDA
- Marketing start
- 2022-07-06
- Substance
- ATENOLOL
- Active strength
- 50 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Atenolol
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ATENOLOL | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 50VV3VW0TI |
| Rxcui | 197381 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-928-26 | Atenolol | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 3 |
| 51655-928-52 | Atenolol | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-928 | ATENOLOL TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 2 | Current NDC, 2 package rows | 20240814_f76d03b8-f8d6-59b8-e053-6394a90a3a3f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51655-928-26 | 51655092826 | 90 TABLET in 1 BOTTLE, PLASTIC (51655-928-26) | 90 tablet | 2022-07-06 | No | No | Historical |
| 51655-928-52 | 51655092852 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-928-52) | 30 tablet | 2022-08-10 | No | No | Historical |