HYDROCHLOROTHIAZIDE
- Product NDC
- 51655-127
- 11-digit product format
- 516550127
- Labeler code
- 51655
- Product ID
- 51655-127_21938319-b511-49a7-a4a0-39e9b649f589
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROCHLOROTHIAZIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals, LLC
- Application
- ANDA079237
- Marketing category
- ANDA
- Marketing start
- 2014-09-14
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 13 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-127 | HYDROCHLOROTHIAZIDE TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 1 | Legacy NDC | 20140924_1c0a4cc8-7fd5-456e-885b-05ec9a0466ea.zip |