quinapril hydrochloride and hydrochlorothiazide
- Product NDC
- 59762-0223
- 11-digit product format
- 597620223
- Labeler code
- 59762
- Product ID
- 59762-0223_46a33cf7-f5c5-4afb-b464-27a36773fe52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- quinapril hydrochloride and hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA020125
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1999-12-28
- Marketing end
- 0000-00-00
- Substance
- QUINAPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
- Active strength
- 20 mg/1; mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59762-0223-1 | 59762022301 | 90 TABLET, FILM COATED in 1 BOTTLE (59762-0223-1) | 1999-12-28 | 0000-00-00 | No | No | Current |