ACCURETIC
- Product NDC
- 0071-0220
- 11-digit product format
- 000710220
- Labeler code
- 0071
- Product ID
- 0071-0220_1d3fab62-2114-4d5b-b07a-9b0f2b5a3efd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- quinapril hydrochloride and hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Parke-Davis Div of Pfizer Inc
- Application
- NDA020125
- Marketing category
- NDA
- 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 |
|---|
| 0071-0220-23 | 00071022023 | 90 TABLET, FILM COATED in 1 BOTTLE (0071-0220-23) | 1999-12-28 | 0000-00-00 | No | No | Current |