Package 31722-176-31
Brand: lisinopril
Generic: lisinoprilPackage Facts
Identity
Package NDC
31722-176-31
Digits Only
3172217631
Product NDC
31722-176
Description
95238 TABLET in 1 CARTON (31722-176-31)
Marketing
Marketing Status
Brand
lisinopril
Generic
lisinopril
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "337644b9-adae-41c1-9a9c-8d879ab355d2", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["197884", "205326", "311353", "311354", "314076", "314077"], "spl_set_id": ["387068e7-7fb9-44f3-ae1c-e45ebc755a3e"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "95238 TABLET in 1 CARTON (31722-176-31)", "package_ndc": "31722-176-31", "marketing_start_date": "20210817"}], "brand_name": "Lisinopril", "product_id": "31722-176_337644b9-adae-41c1-9a9c-8d879ab355d2", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "31722-176", "generic_name": "Lisinopril", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "5 mg/1"}], "application_number": "ANDA075903", "marketing_category": "ANDA", "marketing_start_date": "20210817", "listing_expiration_date": "20261231"}