Atenolol
- Product NDC
- 50090-5408
- 11-digit product format
- 500905408
- Labeler code
- 50090
- Product ID
- 50090-5408_bf5b6387-b343-4c6b-96ef-84c5a904ad89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2010-06-10
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5408-0 | 50090540800 | 30 TABLET in 1 BOTTLE (50090-5408-0) | 30 tablet | 2020-12-11 | 0000-00-00 | No | No | Current |
| 50090-5408-2 | 50090540802 | 100 TABLET in 1 BOTTLE (50090-5408-2) | 100 tablet | 2020-12-11 | 0000-00-00 | No | No | Current |
| 50090-5408-5 | 50090540805 | 90 TABLET in 1 BOTTLE (50090-5408-5) | 90 tablet | 2020-12-11 | 0000-00-00 | No | No | Current |