Chlorthalidone
- Product NDC
- 63629-5259
- 11-digit product format
- 636295259
- Labeler code
- 63629
- Product ID
- 63629-5259_dc56e02a-71ac-432a-8e17-a48e278e1000
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA086831
- Marketing category
- ANDA
- Marketing start
- 1981-02-26
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-5259-1 | 63629525901 | 30 TABLET in 1 BOTTLE (63629-5259-1) | 30 tablet | 2014-03-07 | 0000-00-00 | No | No | Current |
| 63629-5259-2 | 63629525902 | 90 TABLET in 1 BOTTLE (63629-5259-2) | 90 tablet | 2014-03-07 | 0000-00-00 | No | No | Current |
| 63629-5259-3 | 63629525903 | 60 TABLET in 1 BOTTLE (63629-5259-3) | 60 tablet | 2014-03-07 | 0000-00-00 | No | No | Current |
| 63629-5259-4 | 63629525904 | 8 TABLET in 1 BOTTLE (63629-5259-4) | 8 tablet | 2014-03-07 | 0000-00-00 | No | No | Current |