Chlorthalidone
- Product NDC
- 16714-801
- 11-digit product format
- 167140801
- Labeler code
- 16714
- Product ID
- 16714-801_34e75b32-1fad-42a1-ad05-c3dc6f2a91d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA089286
- Marketing category
- ANDA
- Marketing start
- 2018-04-04
- 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-801-01 | 16714080101 | 100 TABLET in 1 BOTTLE (16714-801-01) | 100 tablet | 2018-04-04 | 0000-00-00 | No | No | Current |