Package 44911-0394-1

Brand: sulphur

Generic: sulphur
NDC Package

Package Facts

Identity

Package NDC 44911-0394-1
Digits Only 4491103941
Product NDC 44911-0394
Description

30 mL in 1 BOTTLE, DROPPER (44911-0394-1)

Marketing

Marketing Status
Marketed Since 2016-08-23
Brand sulphur
Generic sulphur
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5add97fb-ea3c-44b3-b068-3a5136924449", "openfda": {"unii": ["70FD1KFU70"], "spl_set_id": ["4c194575-9ac3-436a-9b49-f228146a0bda"], "manufacturer_name": ["Energique, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, DROPPER (44911-0394-1)", "package_ndc": "44911-0394-1", "marketing_start_date": "20160823"}], "brand_name": "Sulphur", "product_id": "44911-0394_5add97fb-ea3c-44b3-b068-3a5136924449", "dosage_form": "LIQUID", "product_ndc": "44911-0394", "generic_name": "Sulphur", "labeler_name": "Energique, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sulphur", "active_ingredients": [{"name": "SULFUR", "strength": "200 [hp_C]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20160823", "listing_expiration_date": "20261231"}