Package 0781-3156-95

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 0781-3156-95
Digits Only 0781315695
Product NDC 0781-3156
Description

10 VIAL, GLASS in 1 CARTON (0781-3156-95) / 100 mL in 1 VIAL, GLASS (0781-3156-06)

Marketing

Marketing Status
Marketed Since 2020-12-06
Brand acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "a309db84-6691-4628-85f9-750bba002be9", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["3b4ab1cf-8642-44f5-b3a2-3f1f7c620ce9"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 CARTON (0781-3156-95)  / 100 mL in 1 VIAL, GLASS (0781-3156-06)", "package_ndc": "0781-3156-95", "marketing_start_date": "20201206"}], "brand_name": "Acetaminophen", "product_id": "0781-3156_a309db84-6691-4628-85f9-750bba002be9", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0781-3156", "generic_name": "acetaminophen", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "10 mg/mL"}], "application_number": "ANDA204052", "marketing_category": "ANDA", "marketing_start_date": "20201206", "listing_expiration_date": "20261231"}