Package 48951-1338-1

Brand: aconitum e tub. 30

Generic: aconitum e tub. 30
NDC Package

Package Facts

Identity

Package NDC 48951-1338-1
Digits Only 4895113381
Product NDC 48951-1338
Product ID 48951-1338_42f33cb7-d6d8-783a-e063-6294a90a3794
Description

10 AMPULE in 1 BOX (48951-1338-1) / 1 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2009-09-01
Brand aconitum e tub. 30
Generic aconitum e tub. 30
Sample Package No

Linked Drug Pages (1)

Aconitum e tub. 30 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "42f33cb7-d6d8-783a-e063-6294a90a3794", "openfda": {"unii": ["U0NQ8555JD"], "spl_set_id": ["8b80552a-6ae3-40ea-bf41-5cd705be04f2"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 BOX (48951-1338-1)  / 1 mL in 1 AMPULE", "package_ndc": "48951-1338-1", "marketing_start_date": "20090901"}], "brand_name": "Aconitum e tub. 30", "product_id": "48951-1338_42f33cb7-d6d8-783a-e063-6294a90a3794", "dosage_form": "LIQUID", "product_ndc": "48951-1338", "generic_name": "Aconitum e tub. 30", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aconitum e tub. 30", "active_ingredients": [{"name": "ACONITUM NAPELLUS", "strength": "30 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}