Package 0220-3030-41

Brand: lachesis mutus

Generic: lachesis muta venom
NDC Package

Package Facts

Identity

Package NDC 0220-3030-41
Digits Only 0220303041
Product NDC 0220-3030
Description

30 [hp_X] in 1 TUBE (0220-3030-41)

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": "0a0e5f97-6e88-9892-e063-6294a90a1a7d", "openfda": {"unii": ["VSW71SS07I"], "spl_set_id": ["861ae219-9a1c-78a0-e053-2991aa0ad056"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_X] in 1 TUBE (0220-3030-41)", "package_ndc": "0220-3030-41", "marketing_start_date": "19830303"}], "brand_name": "Lachesis mutus", "product_id": "0220-3030_0a0e5f97-6e88-9892-e063-6294a90a1a7d", "dosage_form": "PELLET", "product_ndc": "0220-3030", "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": "30 [hp_X]/30[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}