Package 66096-749-08
Brand: spongilla lacustris mt
Generic: spongilla lacustrisPackage Facts
Identity
Package NDC
66096-749-08
Digits Only
6609674908
Product NDC
66096-749
Description
.25 L in 1 BOTTLE (66096-749-08)
Marketing
Marketing Status
Brand
spongilla lacustris mt
Generic
spongilla lacustris
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d449d3d9-49bd-2a4b-e053-2995a90a5a95", "openfda": {"unii": ["6SZ0G98BHM"], "spl_set_id": ["a855d4ca-52ed-4e69-93b5-7304bcc84f73"], "manufacturer_name": ["OHM PHARMA INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".25 L in 1 BOTTLE (66096-749-08)", "package_ndc": "66096-749-08", "marketing_start_date": "20190301"}], "brand_name": "Spongilla lacustris MT", "product_id": "66096-749_d449d3d9-49bd-2a4b-e053-2995a90a5a95", "dosage_form": "TINCTURE", "product_ndc": "66096-749", "generic_name": "Spongilla lacustris", "labeler_name": "OHM PHARMA INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spongilla lacustris MT", "active_ingredients": [{"name": "SPONGILLA LACUSTRIS", "strength": "1 [hp_X]/.25L"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20190301", "listing_expiration_date": "20261231"}