Chlorthalidone
- Product NDC
- 50090-5541
- 11-digit product format
- 500905541
- Labeler code
- 50090
- Product ID
- 50090-5541_4c73341a-4a63-4d50-a085-ce41b596d97f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA207222
- Marketing category
- ANDA
- Marketing start
- 2018-05-28
- Marketing end
- 0000-00-00
- Substance
- CHLORTHALIDONE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 50090-5541-0 | 50090554100 | 100 TABLET in 1 BOTTLE (50090-5541-0) | 100 tablet | 2021-05-10 | 0000-00-00 | No | No | Current |
| 50090-5541-1 | 50090554101 | 30 TABLET in 1 BOTTLE (50090-5541-1) | 30 tablet | 2021-05-10 | 0000-00-00 | No | No | Current |
| 50090-5541-2 | 50090554102 | 90 TABLET in 1 BOTTLE (50090-5541-2) | 90 tablet | 2021-05-10 | 0000-00-00 | No | No | Current |