Package 66096-816-01
Brand: chenopodium
Generic: chenopodiumPackage Facts
Identity
Package NDC
66096-816-01
Digits Only
6609681601
Product NDC
66096-816
Description
6 [hp_C] in 1 PACKAGE (66096-816-01)
Marketing
Marketing Status
Brand
chenopodium
Generic
chenopodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d45e5e2a-0ab6-61de-e053-2995a90a6ba5", "openfda": {"unii": ["4H5RSU087I"], "spl_set_id": ["ee624bf7-96df-424d-a669-01978991bccd"], "manufacturer_name": ["OHM PHARMA INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 PACKAGE (66096-816-01)", "package_ndc": "66096-816-01", "marketing_start_date": "20191101"}], "brand_name": "Chenopodium", "product_id": "66096-816_d45e5e2a-0ab6-61de-e053-2995a90a6ba5", "dosage_form": "PELLET", "product_ndc": "66096-816", "generic_name": "CHENOPODIUM", "labeler_name": "OHM PHARMA INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Chenopodium", "active_ingredients": [{"name": "CHENOPODIUM AMBROSIOIDES", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}