Hydrochlorothiazide
- Product NDC
- 58118-0123
- 11-digit product format
- 581180123
- Labeler code
- 58118
- Product ID
- 58118-0123_adc8df0b-6ce0-550d-e053-2995a90a19b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- Application
- ANDA040907
- Marketing category
- ANDA
- Marketing start
- 2009-07-02
- 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 |
|---|
| 58118-0123 | HYDROCHLOROTHIAZIDE TABLET [CLINICAL SOLUTIONS WHOLESALE, LLC] | 7 | Legacy NDC | 20200827_5451596e-823d-4aaf-96f6-470f034b5f94.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58118-0123-8 | 58118012308 | 30 TABLET in 1 BLISTER PACK (58118-0123-8) | 30 tablet | 2016-06-28 | 0000-00-00 | No | No | Current |