Package 0220-3363-41

Brand: menyanthes trifoliata

Generic: menyanthes trifoliata
NDC Package

Package Facts

Identity

Package NDC 0220-3363-41
Digits Only 0220336341
Product NDC 0220-3363
Description

6 [hp_C] in 1 TUBE (0220-3363-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand menyanthes trifoliata
Generic menyanthes trifoliata
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a1f4673-3e0f-976b-e063-6394a90a5eed", "openfda": {"unii": ["7H0QTZ446K"], "spl_set_id": ["7d79ef71-4418-2564-e053-2991aa0a5255"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-3363-41)", "package_ndc": "0220-3363-41", "marketing_start_date": "19830303"}], "brand_name": "Menyanthes trifoliata", "product_id": "0220-3363_0a1f4673-3e0f-976b-e063-6394a90a5eed", "dosage_form": "PELLET", "product_ndc": "0220-3363", "generic_name": "MENYANTHES TRIFOLIATA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Menyanthes trifoliata", "active_ingredients": [{"name": "MENYANTHES TRIFOLIATA", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}