Package 48951-8434-3

Brand: sun pyrite 17x

Generic: sun pyrite 17x
NDC Package

Package Facts

Identity

Package NDC 48951-8434-3
Digits Only 4895184343
Product NDC 48951-8434
Product ID 48951-8434_3130d5c4-fa48-f6af-e063-6294a90a3708
Description

60 mL in 1 BOTTLE, DROPPER (48951-8434-3)

Marketing

Marketing Status
Marketed Since 2009-09-01
Brand sun pyrite 17x
Generic sun pyrite 17x
Sample Package No

Linked Drug Pages (1)

Sun Pyrite 17X ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3130d5c4-fa48-f6af-e063-6294a90a3708", "openfda": {"unii": ["132N09W4PR"], "spl_set_id": ["3130d5c4-fa47-f6af-e063-6294a90a3708"], "manufacturer_name": ["Uriel Pharmacy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE, DROPPER (48951-8434-3)", "package_ndc": "48951-8434-3", "marketing_start_date": "20090901"}], "brand_name": "Sun Pyrite 17X", "product_id": "48951-8434_3130d5c4-fa48-f6af-e063-6294a90a3708", "dosage_form": "LIQUID", "product_ndc": "48951-8434", "generic_name": "Sun Pyrite 17X", "labeler_name": "Uriel Pharmacy, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sun Pyrite 17X", "active_ingredients": [{"name": "FERROUS DISULFIDE", "strength": "17 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}