Hydrochlorothiazide
- Product NDC
- 50090-2214
- 11-digit product format
- 500902214
- Labeler code
- 50090
- Product ID
- 50090-2214_042ce135-e7e5-41cf-a395-44cf3eff7cd2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040412
- Marketing category
- ANDA
- Marketing start
- 2002-03-29
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2214-0 | Hydrochlorothiazide | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2214 | HYDROCHLOROTHIAZIDE TABLET [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 1 package rows | 20180131_683b8d44-3667-4f5b-8bbb-605ecc3c7154.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2214-0 | 50090221400 | 90 in 1 BOTTLE | Historical |