Package 0143-9787-10

Brand: enalaprilat

Generic: enalaprilat
NDC Package

Package Facts

Identity

Package NDC 0143-9787-10
Digits Only 0143978710
Product NDC 0143-9787
Product ID 0143-9787_bde8c35d-1cf2-42ea-a2a7-c4eb165e6d0d
Description

10 VIAL in 1 CARTON (0143-9787-10) / 1 mL in 1 VIAL (0143-9787-01)

Marketing

Marketing Status
Marketed Since 2008-12-23
Brand enalaprilat
Generic enalaprilat
Sample Package No

Linked Drug Pages (1)

Enalaprilat ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "bde8c35d-1cf2-42ea-a2a7-c4eb165e6d0d", "openfda": {"unii": ["GV0O7ES0R3"], "rxcui": ["1729200", "1729205"], "spl_set_id": ["eabae489-e254-4987-ab90-7cda20a6f856"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9787-10)  / 1 mL in 1 VIAL (0143-9787-01)", "package_ndc": "0143-9787-10", "marketing_start_date": "20081223"}], "brand_name": "Enalaprilat", "product_id": "0143-9787_bde8c35d-1cf2-42ea-a2a7-c4eb165e6d0d", "dosage_form": "INJECTION", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "0143-9787", "generic_name": "enalaprilat", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalaprilat", "active_ingredients": [{"name": "ENALAPRILAT DIHYDRATE", "strength": "1.25 mg/mL"}], "application_number": "ANDA078687", "marketing_category": "ANDA", "marketing_start_date": "20081223", "listing_expiration_date": "20261231"}