Hydrochlorothiazide
- Product NDC
- 60760-199
- 11-digit product format
- 607600199
- Labeler code
- 60760
- Product ID
- 60760-199_f06e6e94-f0e7-7303-e053-2a95a90afa61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-199 | HYDROCHLOROTHIAZIDE TABLET [ST. MARY'S MEDICAL PARK PHARMACY] | 4 | Legacy NDC | 20221223_5f4c576f-cca5-ec7d-e053-2991aa0ad164.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-199-30 | 60760019930 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-199-30) | 30 tablet | 2017-11-21 | 0000-00-00 | No | No | Current |
| 60760-199-90 | 60760019990 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-199-90) | 90 tablet | 2017-11-21 | 0000-00-00 | No | No | Current |