Chlorthalidone
- Product NDC
- 66689-345
- 11-digit product format
- 666890345
- Labeler code
- 66689
- Product ID
- 66689-345_64dab9e7-1ffd-4648-8353-484eac01aaca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- VistaPharm, Inc.
- Application
- ANDA211063
- Marketing category
- ANDA
- Marketing start
- 2019-06-24
- Marketing end
- 2023-05-31
- 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
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66689-345-99 | 66689034599 | 100 TABLET in 1 BOTTLE (66689-345-99) | 100 tablet | 2019-06-24 | 2023-05-31 | No | No | Current |