Package 0220-3030-41
Brand: lachesis mutus
Generic: lachesis muta venomPackage 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
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"}