Chlorthalidone
- Product NDC
- 70934-562
- 11-digit product format
- 709340562
- Labeler code
- 70934
- Product ID
- 70934-562_ac1189b9-7d6e-a79c-e053-2995a90a2f30
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA207222
- Marketing category
- ANDA
- Marketing start
- 2020-02-25
- Marketing end
- 0000-00-00
- Substance
- CHLORTHALIDONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Thiazide-like Diuretic [EPC],Increased Diuresis [PE]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70934-562-30 | 70934056230 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-562-30) | 30 tablet | 2020-02-25 | 0000-00-00 | No | No | Current |