Hydrochlorothiazide
- Product NDC
- 43063-747
- 11-digit product format
- 430630747
- Labeler code
- 43063
- Product ID
- 43063-747_51b60669-eddc-ede8-e063-6294a90ae65c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2013-04-10
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hydrochlorothiazide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCHLOROTHIAZIDE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0J48LPH2TH |
| Rxcui | 197770 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43063-747-01 | Hydrochlorothiazide | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43063-747 | HYDROCHLOROTHIAZIDE TABLET [PD-RX PHARMACEUTICALS, INC.] | 10 | Current NDC, Legacy NDC, 1 package rows | 20241016_27a7e751-8aca-440e-95e4-cfecae1a2465.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-747-01 | 43063074701 | 100 TABLET in 1 BOTTLE, PLASTIC (43063-747-01) | 100 tablet | 2017-02-21 | 0000-00-00 | No | No | Current |