Package 0220-2934-41

Brand: kalmia latifolia

Generic: kalmia latifolia leaf
NDC Package

Package Facts

Identity

Package NDC 0220-2934-41
Digits Only 0220293441
Product NDC 0220-2934
Description

6 [hp_C] in 1 TUBE (0220-2934-41)

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": "0a0dfe8a-78d9-8525-e063-6394a90aff46", "openfda": {"unii": ["79N6542N18"], "spl_set_id": ["68f842b5-0de6-9346-e053-2a91aa0abaac"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-2934-41)", "package_ndc": "0220-2934-41", "marketing_start_date": "19830303"}], "brand_name": "Kalmia latifolia", "product_id": "0220-2934_0a0dfe8a-78d9-8525-e063-6394a90aff46", "dosage_form": "PELLET", "product_ndc": "0220-2934", "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": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}