Hydrochlorothiazide
- Product NDC
- 23155-140
- 11-digit product format
- 231550140
- Labeler code
- 23155
- Product ID
- 23155-140_7a24f8f1-17f8-493a-bede-37314c9681ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc
- Application
- ANDA079237
- Marketing category
- ANDA
- Marketing start
- 2009-06-20
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record