Hydrochlorothiazide
- Product NDC
- 71610-276
- 11-digit product format
- 716100276
- Labeler code
- 71610
- Product ID
- 71610-276_a675bfd4-aacd-4537-b979-c9612aae3c9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA040707
- Marketing category
- ANDA
- Marketing start
- 2017-06-08
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 13 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 71610-276 | HYDROCHLOROTHIAZIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC | 20190516_c31665f6-2504-43e0-9763-9a2e7f174b69.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71610-276-60 | 71610027660 | 90 TABLET in 1 BOTTLE (71610-276-60) | 90 tablet | 2019-05-13 | 0000-00-00 | No | No | Current |