Chlorthalidone
- Product NDC
- 70934-470
- 11-digit product format
- 709340470
- Labeler code
- 70934
- Product ID
- 70934-470_a82421b3-2e28-3d9d-e053-2a95a90a46c2
- 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
- 2019-12-13
- Marketing end
- 0000-00-00
- Substance
- CHLORTHALIDONE
- Active strength
- 25 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 |
|---|
| 70934-470-30 | 70934047030 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-470-30) | 30 tablet | 2019-12-13 | 0000-00-00 | No | No | Current |
| 70934-470-90 | 70934047090 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-470-90) | 90 tablet | 2020-05-19 | 0000-00-00 | No | No | Current |