Package 48951-8433-4

Brand: sun pyrite 8x

Generic: sun pyrite 8x
NDC Package

Package Facts

Identity

Package NDC 48951-8433-4
Digits Only 4895184334
Product NDC 48951-8433
Product ID 48951-8433_2eae3f2d-b712-0f50-e063-6294a90a8349
Description

50 g in 1 BOTTLE (48951-8433-4)

Marketing

Marketing Status
Marketed Since 2009-09-01
Brand sun pyrite 8x
Generic sun pyrite 8x
Sample Package No

Linked Drug Pages (1)

Sun Pyrite 8X ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2eae3f2d-b712-0f50-e063-6294a90a8349", "openfda": {"unii": ["132N09W4PR"], "spl_set_id": ["2eae3f2d-b711-0f50-e063-6294a90a8349"], "manufacturer_name": ["Uriel Pharmacy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE (48951-8433-4)", "package_ndc": "48951-8433-4", "marketing_start_date": "20090901"}], "brand_name": "Sun Pyrite 8X", "product_id": "48951-8433_2eae3f2d-b712-0f50-e063-6294a90a8349", "dosage_form": "POWDER", "product_ndc": "48951-8433", "generic_name": "Sun Pyrite 8X", "labeler_name": "Uriel Pharmacy, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sun Pyrite 8X", "active_ingredients": [{"name": "FERROUS DISULFIDE", "strength": "8 [hp_X]/g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}