Package 48951-5108-1

Brand: helleborus e pl. tota 12

Generic: helleborus e pl. tota 12
NDC Package

Package Facts

Identity

Package NDC 48951-5108-1
Digits Only 4895151081
Product NDC 48951-5108
Product ID 48951-5108_2c532194-0bac-f221-e063-6394a90a4ab9
Description

10 AMPULE in 1 BOX (48951-5108-1) / 1 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2009-09-01
Brand helleborus e pl. tota 12
Generic helleborus e pl. tota 12
Sample Package No

Linked Drug Pages (1)

Helleborus e pl. tota 12 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c532194-0bac-f221-e063-6394a90a4ab9", "openfda": {"unii": ["332Y7EES96"], "spl_set_id": ["6ccb8d0f-6c0b-26ae-e053-2991aa0abeb8"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 BOX (48951-5108-1)  / 1 mL in 1 AMPULE", "package_ndc": "48951-5108-1", "marketing_start_date": "20090901"}], "brand_name": "Helleborus e pl. tota 12", "product_id": "48951-5108_2c532194-0bac-f221-e063-6394a90a4ab9", "dosage_form": "LIQUID", "product_ndc": "48951-5108", "generic_name": "Helleborus e pl. tota 12", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Helleborus e pl. tota 12", "active_ingredients": [{"name": "HELLEBORUS FOETIDUS ROOT", "strength": "12 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}