Hydrochlorothiazide
- Product NDC
- 43063-933
- 11-digit product format
- 430630933
- Labeler code
- 43063
- Product ID
- 43063-933_dafcb77d-8850-615d-e053-2a95a90a4c5a
- 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 |
|---|
| 43063-933 | HYDROCHLOROTHIAZIDE TABLET [PD-RX PHARMACEUTICALS, INC.] | 9 | Legacy NDC | 20241018_b0356653-8467-439a-8fa2-c5aa3d81d475.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-933-01 | 43063093301 | 100 TABLET in 1 BOTTLE, PLASTIC (43063-933-01) | 100 tablet | 2019-01-10 | 0000-00-00 | No | No | Current |