Hydrochlorothiazide
- Product NDC
- 55700-466
- 11-digit product format
- 557000466
- Labeler code
- 55700
- Product ID
- 55700-466_8d57557f-bc74-4ea6-a505-bf7e2a53a9c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2013-04-10
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 50 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