Atenolol
- Product NDC
- 70518-2939
- 11-digit product format
- 705182939
- Labeler code
- 70518
- Product ID
- 70518-2939_eb78f801-add0-3a62-e053-2995a90a3ea1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2020-11-11
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 100 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2939 | ATENOLOL TABLET [REMEDYREPACK INC.] | 9 | Legacy NDC | 20250406_bb02f7f0-8844-4a12-bb9a-69301440dbeb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2939-0 | 70518293900 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2939-0) | 90 tablet | 2020-11-11 | 0000-00-00 | No | No | Current |
| 70518-2939-1 | 70518293901 | 30 TABLET in 1 BLISTER PACK (70518-2939-1) | 30 tablet | 2020-11-19 | 0000-00-00 | No | No | Current |
| 70518-2939-2 | 70518293902 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2939-2) | 90 tablet | 2021-04-05 | 0000-00-00 | No | No | Current |