Package 0220-2932-41

Brand: kalmia latifolia

Generic: kalmia latifolia leaf
NDC Package

Package Facts

Identity

Package NDC 0220-2932-41
Digits Only 0220293241
Product NDC 0220-2932
Description

200 [kp_C] in 1 TUBE (0220-2932-41)

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": "08f2d4aa-73aa-4165-e063-6394a90a747c", "openfda": {"unii": ["79N6542N18"], "spl_set_id": ["8619a4f9-0665-2222-e053-2a91aa0a2d80"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-2932-41)", "package_ndc": "0220-2932-41", "marketing_start_date": "19830303"}], "brand_name": "Kalmia latifolia", "product_id": "0220-2932_08f2d4aa-73aa-4165-e063-6394a90a747c", "dosage_form": "PELLET", "product_ndc": "0220-2932", "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": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}