Atenolol
- Product NDC
- 50090-2923
- 11-digit product format
- 500902923
- Labeler code
- 50090
- Product ID
- 50090-2923_a97585b6-7c97-46fa-999d-f6602babacf0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA073025
- Marketing category
- ANDA
- Marketing start
- 1991-09-17
- 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 |
|---|
| 50090-2923-0 | Atenolol | 100 in 1 BOTTLE | TABLET | 100 | | 11 |
| 50090-2923-7 | Atenolol | 200 in 1 BOTTLE | TABLET | 200 | | 11 |
| 50090-2923-8 | Atenolol | 90 in 1 BOTTLE | TABLET | 90 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2923 | ATENOLOL TABLET [A-S MEDICATION SOLUTIONS] | 11 | Legacy NDC, 3 package rows | 20200122_e6611d33-f4c7-40c4-8db8-6f43c85d444c.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 |
|---|
| 50090-2923-0 | 50090292300 | 100 TABLET in 1 BOTTLE (50090-2923-0) | 100 tablet | 2017-03-23 | 0000-00-00 | No | No | Current |
| 50090-2923-7 | 50090292307 | 200 TABLET in 1 BOTTLE (50090-2923-7) | 200 tablet | 2017-03-21 | 0000-00-00 | No | No | Current |
| 50090-2923-8 | 50090292308 | 90 TABLET in 1 BOTTLE (50090-2923-8) | 90 tablet | 2017-03-16 | 0000-00-00 | No | No | Current |