Hydrochlorothiazide
- Product NDC
- 43063-755
- 11-digit product format
- 430630755
- Labeler code
- 43063
- Product ID
- 43063-755_e890bee0-1651-2a74-e053-2995a90a3e2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA040412
- Marketing category
- ANDA
- Marketing start
- 2002-03-29
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43063-755 | HYDROCHLOROTHIAZIDE TABLET [PD-RX PHARMACEUTICALS, INC.] | 18 | Legacy NDC | 20241016_70c516da-d9bd-4d89-9f34-4a2be28ce07b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-755-01 | 43063075501 | 100 TABLET in 1 BOTTLE, PLASTIC (43063-755-01) | 100 tablet | 2017-05-23 | 0000-00-00 | No | No | Current |
| 43063-755-07 | 43063075507 | 7 TABLET in 1 BOTTLE, PLASTIC (43063-755-07) | 7 tablet | 2018-03-07 | 0000-00-00 | No | No | Current |
| 43063-755-30 | 43063075530 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-755-30) | 30 tablet | 2017-06-15 | 0000-00-00 | No | No | Current |
| 43063-755-60 | 43063075560 | 60 TABLET in 1 BOTTLE, PLASTIC (43063-755-60) | 60 tablet | 2017-05-26 | 0000-00-00 | No | No | Current |
| 43063-755-90 | 43063075590 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-755-90) | 90 tablet | 2017-04-14 | 0000-00-00 | No | No | Current |
| 43063-755-95 | 43063075595 | 1000 TABLET in 1 BOTTLE, PLASTIC (43063-755-95) | 1000 tablet | 2017-04-14 | 0000-00-00 | No | No | Current |