Hydrochlorothiazide
- Product NDC
- 45865-532
- 11-digit product format
- 458650532
- Labeler code
- 45865
- Product ID
- 45865-532_7176c8c1-1f7c-88c1-e053-2a95a90a89f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Medsource Pharmaceuticals
- 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
- 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 |
|---|
| 45865-532-30 | Hydrochlorothiazide | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 45865-532-49 | Hydrochlorothiazide | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45865-532 | HYDROCHLOROTHIAZIDE TABLET [MEDSOURCE PHARMACEUTICALS] | 1 | Legacy NDC, 2 package rows | 20180723_7176c8c1-1f7b-88c1-e053-2a95a90a89f0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 45865-532-30 | 45865053230 | 30 in 1 BOTTLE | Historical |
| 45865-532-49 | 45865053249 | 100 in 1 BOTTLE | Historical |