Lisinopril and hydrochlorothiazide
- Product NDC
- 68788-6972
- 11-digit product format
- 687886972
- Labeler code
- 68788
- Product ID
- 68788-6972_8b001258-4820-4090-a5d9-81ef589bc9b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril and hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076194
- Marketing category
- ANDA
- Marketing start
- 2017-06-07
- Marketing end
- 0000-00-00
- Substance
- LISINOPRIL; HYDROCHLOROTHIAZIDE
- Active strength
- 10 mg/1; mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record