Package 0220-1796-41

Brand: drosera

Generic: drosera rotundifolia
NDC Package

Package Facts

Identity

Package NDC 0220-1796-41
Digits Only 0220179641
Product NDC 0220-1796
Description

30 [hp_C] in 1 TUBE (0220-1796-41)

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": "f2b8c004-abc7-015b-e053-2a95a90a40e8", "openfda": {"unii": ["QR44N9XPJQ"], "spl_set_id": ["858ea93a-9293-da7f-e053-2a91aa0af184"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-1796-41)", "package_ndc": "0220-1796-41", "marketing_start_date": "19830303"}], "brand_name": "Drosera", "product_id": "0220-1796_f2b8c004-abc7-015b-e053-2a95a90a40e8", "dosage_form": "PELLET", "product_ndc": "0220-1796", "generic_name": "DROSERA ROTUNDIFOLIA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Drosera", "active_ingredients": [{"name": "DROSERA ROTUNDIFOLIA", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}