Chlorthalidone
- Product NDC
- 50090-0144
- 11-digit product format
- 500900144
- Labeler code
- 50090
- Product ID
- 50090-0144_e34160f6-cfb2-4ea7-b3ed-f13a465b6a36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2020-12-31
- 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 |
|---|
| 50090-0144-1 | 50090014401 | 30 TABLET in 1 BOTTLE, PLASTIC (50090-0144-1) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0144-2 | 50090014402 | 90 TABLET in 1 BOTTLE, PLASTIC (50090-0144-2) | 90 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |