Package 0220-2927-41
Brand: kalmia latifolia
Generic: kalmia latifolia leafPackage Facts
Identity
Package NDC
0220-2927-41
Digits Only
0220292741
Product NDC
0220-2927
Description
9 [hp_C] in 1 TUBE (0220-2927-41)
Marketing
Marketing Status
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": "0a0dfe8a-78d8-8525-e063-6394a90aff46", "openfda": {"unii": ["79N6542N18"], "spl_set_id": ["860b969e-d3c0-b7df-e053-2a91aa0af7b9"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-2927-41)", "package_ndc": "0220-2927-41", "marketing_start_date": "19830303"}], "brand_name": "Kalmia latifolia", "product_id": "0220-2927_0a0dfe8a-78d8-8525-e063-6394a90aff46", "dosage_form": "PELLET", "product_ndc": "0220-2927", "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": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}