Hydrochlorothiazide
- Product NDC
- 50090-2727
- 11-digit product format
- 500902727
- Labeler code
- 50090
- Product ID
- 50090-2727_330a35f7-a979-4541-b5a7-41f441282aa7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2013-04-10
- 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
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2727 | HYDROCHLOROTHIAZIDE TABLET [A-S MEDICATION SOLUTIONS] | 17 | Legacy NDC | 20240425_457e7ec7-d012-4ae9-abf0-2eec12050ca5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2727-0 | 50090272700 | 30 TABLET in 1 BOTTLE (50090-2727-0) | 30 tablet | 2017-01-04 | 0000-00-00 | No | No | Current |
| 50090-2727-1 | 50090272701 | 100 TABLET in 1 BOTTLE (50090-2727-1) | 100 tablet | 2016-12-27 | 0000-00-00 | No | No | Current |
| 50090-2727-8 | 50090272708 | 200 TABLET in 1 BOTTLE (50090-2727-8) | 200 tablet | 2017-03-21 | 0000-00-00 | No | No | Current |