Package 85816-5121-1
Brand: bm berberis vulgaris
Generic: berberis vulgarisPackage Facts
Identity
Package NDC
85816-5121-1
Digits Only
8581651211
Product NDC
85816-5121
Description
30 mL in 1 BOTTLE, GLASS (85816-5121-1)
Marketing
Marketing Status
Brand
bm berberis vulgaris
Generic
berberis vulgaris
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38db12e8-d83a-2f27-e063-6394a90a2f36", "openfda": {"unii": ["1TH8Q20J0U"], "spl_set_id": ["38db12e8-d839-2f27-e063-6394a90a2f36"], "manufacturer_name": ["BM Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, GLASS (85816-5121-1)", "package_ndc": "85816-5121-1", "marketing_start_date": "20150101"}], "brand_name": "BM Berberis Vulgaris", "product_id": "85816-5121_38db12e8-d83a-2f27-e063-6394a90a2f36", "dosage_form": "TINCTURE", "product_ndc": "85816-5121", "generic_name": "Berberis Vulgaris", "labeler_name": "BM Private Limited", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BM Berberis Vulgaris", "active_ingredients": [{"name": "BERBERIS VULGARIS ROOT BARK", "strength": "1 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20150101", "listing_expiration_date": "20261231"}