Hydrochlorothiazide
- Product NDC
- 51655-502
- 11-digit product format
- 516550502
- Labeler code
- 51655
- Product ID
- 51655-502_490f8e1a-5021-5426-e063-6394a90a8159
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2015-03-06
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 12.5 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 | 12.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0J48LPH2TH |
| Rxcui | 429503 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
NDC, Effective, Action table| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|
| 51655-502-26 | 2023-04-12 | C162847 | 48780-1 | 9d75b9d0-86f5-f424-e053-dadaa90a57ce | HYDROCHLOROTHIAZIDE TABLETS, USP 12.5 mg, 25 mg and 50 mg Rx only |
| 51655-502-52 | 2023-04-12 | C162847 | 48780-1 | 9d75b9d0-86f5-f424-e053-dadaa90a57ce | HYDROCHLOROTHIAZIDE TABLETS, USP 12.5 mg, 25 mg and 50 mg Rx only |
| 51655-502-26 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-86f5-f424-e053-dadaa90a57ce | HYDROCHLOROTHIAZIDE TABLETS, USP 12.5 mg, 25 mg and 50 mg Rx only |
| 51655-502-52 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-86f5-f424-e053-dadaa90a57ce | HYDROCHLOROTHIAZIDE TABLETS, USP 12.5 mg, 25 mg and 50 mg Rx only |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-502-26 | Hydrochlorothiazide | 90 in 1 BOTTLE, DISPENSING | TABLET | 90 | | 4 |
| 51655-502-52 | Hydrochlorothiazide | 30 in 1 BOTTLE, DISPENSING | TABLET | 30 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-502 | HYDROCHLOROTHIAZIDE TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 3 | Current NDC, Legacy NDC, 2 package rows | 20230413_57a2f9bd-8ca5-437e-b911-5207f94cc6ba.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51655-502-26 | 51655050226 | 90 TABLET in 1 BOTTLE, DISPENSING (51655-502-26) | 90 tablet | 2015-03-06 | No | No | Current |
| 51655-502-52 | 51655050252 | 30 TABLET in 1 BOTTLE, DISPENSING (51655-502-52) | 30 tablet | 2015-03-06 | No | No | Current |