Atenolol and Chlorthalidone
- Product NDC
- 68071-3065
- 11-digit product format
- 680713065
- Labeler code
- 68071
- Product ID
- 68071-3065_bb12c51c-4b2e-02c5-e053-2995a90ac05b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol and Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA073665
- Marketing category
- ANDA
- Marketing start
- 1992-08-01
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL; CHLORTHALIDONE
- Active strength
- 50 mg/1; mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Thiazide-like Diuretic [EPC],Increased Diuresis [PE]
- 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 |
|---|
| 68071-3065-3 | 68071306503 | 30 TABLET in 1 BOTTLE (68071-3065-3) | 30 tablet | 2017-03-14 | 0000-00-00 | No | No | Current |
| 68071-3065-6 | 68071306506 | 60 TABLET in 1 BOTTLE (68071-3065-6) | 60 tablet | 2017-03-14 | 0000-00-00 | No | No | Current |
| 68071-3065-9 | 68071306509 | 90 TABLET in 1 BOTTLE (68071-3065-9) | 90 tablet | 2017-03-14 | 0000-00-00 | No | No | Current |