Hydrochlorothiazide
- Product NDC
- 50090-2744
- 11-digit product format
- 500902744
- Labeler code
- 50090
- Product ID
- 50090-2744_c312e30e-48de-4bec-bb3a-dc67c4300811
- 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
- 2022-12-31
- 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 |
|---|
| 50090-2744 | HYDROCHLOROTHIAZIDE TABLET [A-S MEDICATION SOLUTIONS] | 16 | Legacy NDC | 20240425_42c36911-1cb6-4f24-9daa-b0b29a677afc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2744-0 | 50090274400 | 90 TABLET in 1 BOTTLE (50090-2744-0) | 90 tablet | 2017-01-04 | 0000-00-00 | No | No | Current |