Atenolol
- Product NDC
- 70518-3007
- 11-digit product format
- 705183007
- Labeler code
- 70518
- Product ID
- 70518-3007_e65dd34f-b938-4730-e053-2995a90a4431
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2021-02-02
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3007-0 | 70518300700 | 30 TABLET in 1 BLISTER PACK (70518-3007-0) | 30 tablet | 2021-02-02 | 0000-00-00 | No | No | Current |
| 70518-3007-1 | 70518300701 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3007-1) | 90 tablet | 2021-04-01 | 0000-00-00 | No | No | Current |
| 70518-3007-2 | 70518300702 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3007-2) | 90 tablet | 2022-08-16 | 0000-00-00 | No | No | Current |