CHLORTHALIDONE
- Product NDC
- 55801-146
- 11-digit product format
- 558010146
- Labeler code
- 55801
- Product ID
- 55801-146_994b47c3-79bf-21ba-e053-2995a90ad21d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORTHALIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Appco Pharma LLC
- Application
- ANDA210742
- Marketing category
- ANDA
- Marketing start
- 2018-10-22
- Marketing end
- 0000-00-00
- Substance
- CHLORTHALIDONE
- Active strength
- 50 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 55801-146-01 | 55801014601 | 100 TABLET in 1 BOTTLE (55801-146-01) | 100 tablet | 2018-10-22 | 0000-00-00 | No | No | Current |
| 55801-146-02 | 55801014602 | 1000 TABLET in 1 BOTTLE (55801-146-02) | 1000 tablet | 2018-10-22 | 0000-00-00 | No | No | Current |