Hydrochlorothiazide
- Product NDC
- 52959-132
- 11-digit product format
- 529590132
- Labeler code
- 52959
- Product ID
- 52959-132_150cd716-8f3b-4890-807f-8a54ecc9e183
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA040807
- Marketing category
- ANDA
- Marketing start
- 2010-08-20
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52959-132-00 | Hydrochlorothiazide | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 52959-132-07 | Hydrochlorothiazide | 7 in 1 BOTTLE | TABLET | 7 | | 1 |
| 52959-132-30 | Hydrochlorothiazide | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 52959-132-60 | Hydrochlorothiazide | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| HYDROCHLOROTHIAZIDE | ACTIVE INGREDIENT | 0J48LPH2TH | HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| HYDROCHLOROTHIAZIDE | ACTIVE MOIETY | 0J48LPH2TH | HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| DIBASIC CALCIUM PHOSPHATE DIHYDRATE | INACTIVE INGREDIENT | O7TSZ97GEP | HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52959-132 | HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | Legacy NDC, 4 package rows | 20111118_8a3e269e-d803-4737-b6cd-6226b4d8f2fc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 52959-132-00 | 52959013200 | 100 in 1 BOTTLE | Historical |
| 52959-132-07 | 52959013207 | 7 in 1 BOTTLE | Historical |
| 52959-132-30 | 52959013230 | 30 in 1 BOTTLE | Historical |
| 52959-132-60 | 52959013260 | 60 in 1 BOTTLE | Historical |