Atenolol and Chlorthalidone
- Product NDC
- 70518-3550
- 11-digit product format
- 705183550
- Labeler code
- 70518
- Product ID
- 70518-3550_ea607725-77b6-77ef-e053-2a95a90a0f9c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol and Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA215560
- Marketing category
- ANDA
- Marketing start
- 2022-10-06
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL; CHLORTHALIDONE
- Active strength
- 100 mg/1; mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide-like Diuretic [EPC], 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 |
|---|
| 70518-3550-0 | 70518355000 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3550-0) | 90 tablet | 2022-10-06 | 0000-00-00 | No | No | Current |