Atenolol and Chlorthalidone
- Product NDC
- 70518-2044
- 11-digit product format
- 705182044
- Labeler code
- 70518
- Product ID
- 70518-2044_87b17112-3911-ceac-e053-2a95a90aebb0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol and Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA073665
- Marketing category
- ANDA
- Marketing start
- 2019-04-29
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL; CHLORTHALIDONE
- Active strength
- 100 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record