Package 48951-7214-2

Brand: oxalis 1x

Generic: oxalis 1x
NDC Package

Package Facts

Identity

Package NDC 48951-7214-2
Digits Only 4895172142
Product NDC 48951-7214
Product ID 48951-7214_2c907346-28ec-f243-e063-6294a90ae572
Description

30 g in 1 TUBE (48951-7214-2)

Marketing

Marketing Status
Marketed Since 2009-09-01
Brand oxalis 1x
Generic oxalis 1x
Sample Package No

Linked Drug Pages (1)

Oxalis 1X ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2c907346-28ec-f243-e063-6294a90ae572", "openfda": {"unii": ["3STW243384"], "spl_set_id": ["2c907346-28eb-f243-e063-6294a90ae572"], "manufacturer_name": ["Uriel Pharmacy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 g in 1 TUBE (48951-7214-2)", "package_ndc": "48951-7214-2", "marketing_start_date": "20090901"}], "brand_name": "Oxalis 1X", "product_id": "48951-7214_2c907346-28ec-f243-e063-6294a90ae572", "dosage_form": "OINTMENT", "product_ndc": "48951-7214", "generic_name": "Oxalis 1X", "labeler_name": "Uriel Pharmacy, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Oxalis 1X", "active_ingredients": [{"name": "OXALIS STRICTA WHOLE", "strength": "1 [hp_X]/g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}