Hydrochlorothiazide
- Product NDC
- 70518-0210
- 11-digit product format
- 705180210
- Labeler code
- 70518
- Product ID
- 70518-0210_e701c8c8-d9ee-3740-e053-2995a90a0850
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2017-02-09
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- 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 |
|---|
| 70518-0210-0 | 70518021000 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-0210-0) | 100 tablet | 2017-02-09 | 0000-00-00 | No | No | Current |
| 70518-0210-1 | 70518021001 | 30 TABLET in 1 BLISTER PACK (70518-0210-1) | 30 tablet | 2017-03-03 | 0000-00-00 | No | No | Current |
| 70518-0210-2 | 70518021002 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0210-2) | 90 tablet | 2017-04-24 | 0000-00-00 | No | No | Current |
| 70518-0210-3 | 70518021003 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-0210-3) | 30 tablet | 2017-05-12 | 0000-00-00 | No | No | Current |