hydrochlorothiazide
- Product NDC
- 61919-695
- 11-digit product format
- 619190695
- Labeler code
- 61919
- Product ID
- 61919-695_e9adac07-9fa0-da45-e053-2a95a90ad477
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct RX
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2018-11-09
- 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
- 2023-12-31
- 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 |
|---|
| 61919-695-30 | hydrochlorothiazide | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 61919-695-90 | 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 |
|---|
| 61919-695 | HYDROCHLOROTHIAZIDE TABLET [DIRECT RX] | 3 | Legacy NDC, 2 package rows | 20230511_7a40a207-fcaa-4e6f-e053-2a91aa0aa29f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-695-30 | 61919069530 | 30 TABLET in 1 BOTTLE (61919-695-30) | 30 tablet | 2018-11-09 | 0000-00-00 | No | No | Current |
| 61919-695-90 | 61919069590 | 90 TABLET in 1 BOTTLE (61919-695-90) | 90 tablet | 2018-11-09 | 0000-00-00 | No | No | Current |