Package 0220-1792-41

Brand: drosera

Generic: drosera rotundifolia
NDC Package

Package Facts

Identity

Package NDC 0220-1792-41
Digits Only 0220179241
Product NDC 0220-1792
Description

12 [hp_C] in 1 TUBE (0220-1792-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand drosera
Generic drosera rotundifolia
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0ca58e-c4fb-ab5b-e063-6394a90ab630", "openfda": {"unii": ["QR44N9XPJQ"], "spl_set_id": ["858e5938-8a95-7a2b-e053-2a91aa0a13d2"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 [hp_C] in 1 TUBE (0220-1792-41)", "package_ndc": "0220-1792-41", "marketing_start_date": "19830303"}], "brand_name": "Drosera", "product_id": "0220-1792_0a0ca58e-c4fb-ab5b-e063-6394a90ab630", "dosage_form": "PELLET", "product_ndc": "0220-1792", "generic_name": "DROSERA ROTUNDIFOLIA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Drosera", "active_ingredients": [{"name": "DROSERA ROTUNDIFOLIA", "strength": "12 [hp_C]/12[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}