Microzide
- Product NDC
- 0023-6154
- 11-digit product format
- 000236154
- Labeler code
- 0023
- Product ID
- 0023-6154_07a7bc5e-e15d-4164-9510-e142c7214367
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Allergan, Inc.
- Application
- NDA020504
- Marketing category
- NDA
- Marketing start
- 1996-12-27
- Marketing end
- 2020-08-31
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 13 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record