Package 31722-205-24

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 31722-205-24
Digits Only 3172220524
Product NDC 31722-205
Product ID 31722-205_e8c546a7-cc7c-a8de-e053-2995a90aad43
Description

24 VIAL, SINGLE-DOSE in 1 CARTON (31722-205-24) / 100 mL in 1 VIAL, SINGLE-DOSE (31722-205-31)

Marketing

Marketing Status
Marketed Since 2022-07-27
Brand acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "e8c546a7-cc7c-a8de-e053-2995a90aad43", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["1c8fef8f-2ff5-4bea-bccb-90c2c8544c21"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 VIAL, SINGLE-DOSE in 1 CARTON (31722-205-24)  / 100 mL in 1 VIAL, SINGLE-DOSE (31722-205-31)", "package_ndc": "31722-205-24", "marketing_start_date": "20220727"}], "brand_name": "Acetaminophen", "product_id": "31722-205_e8c546a7-cc7c-a8de-e053-2995a90aad43", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "31722-205", "generic_name": "Acetaminophen", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "10 mg/mL"}], "application_number": "ANDA216617", "marketing_category": "ANDA", "marketing_start_date": "20220727", "listing_expiration_date": "20261231"}