Chlorthalidone
- Product NDC
- 16714-800
- 11-digit product format
- 167140800
- Labeler code
- 16714
- Product ID
- 16714-800_eeb7d799-0912-e4be-e053-2995a90ae36c
- 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
- 2022-12-31
- 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 |
|---|
| 16714-800-01 | 16714080001 | 100 TABLET in 1 BOTTLE (16714-800-01) | 100 tablet | 2018-04-04 | 0000-00-00 | No | No | Current |