HYDROCHLOROTHIAZIDE
- Product NDC
- 70518-2666
- 11-digit product format
- 705182666
- Labeler code
- 70518
- Product ID
- 70518-2666_dc88f8e4-1d16-f204-e053-2a95a90ad6b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROCHLOROTHIAZIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040702
- Marketing category
- ANDA
- Marketing start
- 2020-03-31
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 13 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2666 | HYDROCHLOROTHIAZIDE TABLET [REMEDYREPACK INC.] | 11 | Legacy NDC | 20250327_1da05129-2d1d-462b-a64f-2c82fac735f9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2666-0 | 70518266600 | 30 TABLET in 1 BLISTER PACK (70518-2666-0) | 30 tablet | 2020-03-31 | 0000-00-00 | No | No | Current |
| 70518-2666-1 | 70518266601 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2666-1) | 90 tablet | 2021-07-27 | 0000-00-00 | No | No | Current |