Package 0220-3013-41

Brand: lachesis mutus

Generic: lachesis muta venom
NDC Package

Package Facts

Identity

Package NDC 0220-3013-41
Digits Only 0220301341
Product NDC 0220-3013
Description

6 [hp_C] in 1 TUBE (0220-3013-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand lachesis mutus
Generic lachesis muta venom
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f52bfe56-ceab-53ee-e053-2a95a90af5c4", "openfda": {"unii": ["VSW71SS07I"], "spl_set_id": ["861ab013-a8b5-816a-e053-2a91aa0abc1b"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-3013-41)", "package_ndc": "0220-3013-41", "marketing_start_date": "19830303"}], "brand_name": "Lachesis mutus", "product_id": "0220-3013_f52bfe56-ceab-53ee-e053-2a95a90af5c4", "dosage_form": "PELLET", "product_ndc": "0220-3013", "generic_name": "LACHESIS MUTA VENOM", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lachesis mutus", "active_ingredients": [{"name": "LACHESIS MUTA VENOM", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}