Package 48951-7221-5

Brand: oxalis 20%

Generic: oxalis 20%
NDC Package

Package Facts

Identity

Package NDC 48951-7221-5
Digits Only 4895172215
Product NDC 48951-7221
Product ID 48951-7221_3b52ff8d-4b88-d598-e063-6294a90aebd0
Description

60 g in 1 TUBE (48951-7221-5)

Marketing

Marketing Status
Marketed Since 2009-09-01
Brand oxalis 20%
Generic oxalis 20%
Sample Package No

Linked Drug Pages (1)

Oxalis 20% ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3b52ff8d-4b88-d598-e063-6294a90aebd0", "openfda": {"unii": ["3STW243384"], "spl_set_id": ["3b52ff8d-4b87-d598-e063-6294a90aebd0"], "manufacturer_name": ["Uriel Pharmcy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 g in 1 TUBE (48951-7221-5)", "package_ndc": "48951-7221-5", "marketing_start_date": "20090901"}], "brand_name": "Oxalis 20%", "product_id": "48951-7221_3b52ff8d-4b88-d598-e063-6294a90aebd0", "dosage_form": "OINTMENT", "product_ndc": "48951-7221", "generic_name": "Oxalis 20%", "labeler_name": "Uriel Pharmcy, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Oxalis 20%", "active_ingredients": [{"name": "OXALIS STRICTA WHOLE", "strength": "1 [hp_X]/g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}