Package 0220-2931-41

Brand: kalmia latifolia

Generic: kalmia latifolia leaf
NDC Package

Package Facts

Identity

Package NDC 0220-2931-41
Digits Only 0220293141
Product NDC 0220-2931
Description

30 [hp_C] in 1 TUBE (0220-2931-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand kalmia latifolia
Generic kalmia latifolia leaf
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f9155d23-35bf-0802-e053-6294a90a50af", "openfda": {"unii": ["79N6542N18"], "spl_set_id": ["861970e9-c5d4-2569-e053-2a91aa0a94c2"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-2931-41)", "package_ndc": "0220-2931-41", "marketing_start_date": "19830303"}], "brand_name": "Kalmia latifolia", "product_id": "0220-2931_f9155d23-35bf-0802-e053-6294a90a50af", "dosage_form": "PELLET", "product_ndc": "0220-2931", "generic_name": "KALMIA LATIFOLIA LEAF", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kalmia latifolia", "active_ingredients": [{"name": "KALMIA LATIFOLIA LEAF", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}