HYDROCHLOROTHIAZIDE
- Product NDC
- 12634-445
- 11-digit product format
- 126340445
- Labeler code
- 12634
- Product ID
- 12634-445_f603db60-428d-470d-96d6-2c9486dfa784
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROCHLOROTHIAZIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Apotheca, Inc.
- Application
- ANDA084325
- Marketing category
- ANDA
- Marketing start
- 1996-12-21
- 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
- 2018-12-31
- 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 |
|---|
| 12634-445-50 | HYDROCHLOROTHIAZIDE | 50 in 1 BOTTLE | TABLET | 50 | | 1 |
| 12634-445-60 | HYDROCHLOROTHIAZIDE | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 12634-445-71 | HYDROCHLOROTHIAZIDE | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 12634-445-78 | HYDROCHLOROTHIAZIDE | 28 in 1 BOTTLE | TABLET | 28 | | 1 |
| 12634-445-79 | HYDROCHLOROTHIAZIDE | 25 in 1 BOTTLE | TABLET | 25 | | 1 |
| 12634-445-85 | HYDROCHLOROTHIAZIDE | 15 in 1 BOTTLE | TABLET | 15 | | 1 |
| 12634-445-90 | HYDROCHLOROTHIAZIDE | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
| 12634-445-91 | HYDROCHLOROTHIAZIDE | 1 in 1 BLISTER PACK | TABLET | 1 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| HYDROCHLOROTHIAZIDE | ACTIVE INGREDIENT | 0J48LPH2TH | HYDROCHLOROTHIAZIDE TABLET [APOTHECA, INC.] | 1 | |
| HYDROCHLOROTHIAZIDE | ACTIVE MOIETY | 0J48LPH2TH | HYDROCHLOROTHIAZIDE TABLET [APOTHECA, INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | HYDROCHLOROTHIAZIDE TABLET [APOTHECA, INC.] | 1 | |
| D&C YELLOW NO. 10 | INACTIVE INGREDIENT | 35SW5USQ3G | HYDROCHLOROTHIAZIDE TABLET [APOTHECA, INC.] | 1 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | HYDROCHLOROTHIAZIDE TABLET [APOTHECA, INC.] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | HYDROCHLOROTHIAZIDE TABLET [APOTHECA, INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | HYDROCHLOROTHIAZIDE TABLET [APOTHECA, INC.] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | HYDROCHLOROTHIAZIDE TABLET [APOTHECA, INC.] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | HYDROCHLOROTHIAZIDE TABLET [APOTHECA, INC.] | 1 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | HYDROCHLOROTHIAZIDE TABLET [APOTHECA, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 12634-445 | HYDROCHLOROTHIAZIDE TABLET [APOTHECA, INC.] | 1 | Legacy NDC, 8 package rows | 20100505_2c4954a3-35dd-4ea1-ad32-0044d6db1665.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 12634-445-50 | 12634044550 | 50 in 1 BOTTLE | Historical |
| 12634-445-60 | 12634044560 | 60 in 1 BOTTLE | Historical |
| 12634-445-71 | 12634044571 | 30 in 1 BOTTLE | Historical |
| 12634-445-78 | 12634044578 | 28 in 1 BOTTLE | Historical |
| 12634-445-79 | 12634044579 | 25 in 1 BOTTLE | Historical |
| 12634-445-85 | 12634044585 | 15 in 1 BOTTLE | Historical |
| 12634-445-90 | 12634044590 | 90 in 1 BOTTLE | Historical |
| 12634-445-91 | 12634044591 | 1 in 1 BLISTER PACK | Historical |