Atenolol
- Product NDC
- 63629-6443
- 11-digit product format
- 636296443
- Labeler code
- 63629
- Product ID
- 63629-6443_eda8d4d2-1eeb-4251-93a4-205df1388c59
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074056
- Marketing category
- ANDA
- Marketing start
- 2004-11-16
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63629-6443-1 | 63629644301 | 30 TABLET in 1 BOTTLE (63629-6443-1) | 30 tablet | 2015-08-28 | 0000-00-00 | No | No | Current |
| 63629-6443-2 | 63629644302 | 90 TABLET in 1 BOTTLE (63629-6443-2) | 90 tablet | 2015-08-28 | 0000-00-00 | No | No | Current |