Chlorthalidone
- Product NDC
- 71335-1708
- 11-digit product format
- 713351708
- Labeler code
- 71335
- Product ID
- 71335-1708_10e2c035-7131-4de2-ace0-1a9f27db2fdc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211063
- Marketing category
- ANDA
- Marketing start
- 2019-06-24
- Marketing end
- 2023-05-31
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1708-1 | 71335170801 | 30 TABLET in 1 BOTTLE (71335-1708-1) | 30 tablet | 2020-10-20 | 2023-05-31 | No | No | Current |
| 71335-1708-2 | 71335170802 | 90 TABLET in 1 BOTTLE (71335-1708-2) | 90 tablet | 2020-10-16 | 2023-05-31 | No | No | Current |
| 71335-1708-3 | 71335170803 | 60 TABLET in 1 BOTTLE (71335-1708-3) | 60 tablet | 2022-03-10 | 2023-05-31 | No | No | Current |
| 71335-1708-4 | 71335170804 | 8 TABLET in 1 BOTTLE (71335-1708-4) | 8 tablet | 2022-03-10 | 2023-05-31 | No | No | Current |
| 71335-1708-5 | 71335170805 | 100 TABLET in 1 BOTTLE (71335-1708-5) | 100 tablet | 2021-07-07 | 2023-05-31 | No | No | Current |