Chlorthalidone
- Product NDC
- 70934-938
- 11-digit product format
- 709340938
- Labeler code
- 70934
- Product ID
- 70934-938_f162b1a8-65b2-13a8-e053-2a95a90a3f13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA214129
- Marketing category
- ANDA
- Marketing start
- 2021-12-27
- Marketing end
- 2023-01-31
- Substance
- CHLORTHALIDONE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 70934-938-90 | 70934093890 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-938-90) | 90 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |