Package 48951-7224-5

Brand: oxalis 5x

Generic: oxalis 5x
NDC Package

Package Facts

Identity

Package NDC 48951-7224-5
Digits Only 4895172245
Product NDC 48951-7224
Description

60 g in 1 TUBE (48951-7224-5)

Marketing

Marketing Status
Marketed Since 2009-09-01
Brand oxalis 5x
Generic oxalis 5x
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "49de8ed6-b5e9-e8ea-e063-6394a90ad071", "openfda": {"unii": ["3STW243384"], "spl_set_id": ["49de8ed6-b5e8-e8ea-e063-6394a90ad071"], "manufacturer_name": ["Uriel Pharmacy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 g in 1 TUBE (48951-7224-5)", "package_ndc": "48951-7224-5", "marketing_start_date": "20090901"}], "brand_name": "Oxalis 5X", "product_id": "48951-7224_49de8ed6-b5e9-e8ea-e063-6394a90ad071", "dosage_form": "OINTMENT", "product_ndc": "48951-7224", "generic_name": "Oxalis 5X", "labeler_name": "Uriel Pharmacy, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Oxalis 5X", "active_ingredients": [{"name": "OXALIS STRICTA WHOLE", "strength": "5 [hp_X]/g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20271231"}