Atenolol
- Product NDC
- 70518-2866
- 11-digit product format
- 705182866
- Labeler code
- 70518
- Product ID
- 70518-2866_d773c7c7-809b-c812-e053-2a95a90a6915
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2020-09-02
- 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
- 2023-12-31
- 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 |
|---|
| 70518-2866-0 | 70518286600 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-2866-0) | 100 tablet | 2020-09-02 | 0000-00-00 | No | No | Current |