Package 0220-3029-41

Brand: lachesis mutus

Generic: lachesis muta venom
NDC Package

Package Facts

Identity

Package NDC 0220-3029-41
Digits Only 0220302941
Product NDC 0220-3029
Description

10 [hp_M] in 1 TUBE (0220-3029-41)

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": "0a0e30cc-ad7d-8cf3-e063-6394a90a974d", "openfda": {"unii": ["VSW71SS07I"], "spl_set_id": ["861b7422-9b16-120e-e053-2991aa0aa91b"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 [hp_M] in 1 TUBE (0220-3029-41)", "package_ndc": "0220-3029-41", "marketing_start_date": "19830303"}], "brand_name": "Lachesis mutus", "product_id": "0220-3029_0a0e30cc-ad7d-8cf3-e063-6394a90a974d", "dosage_form": "PELLET", "product_ndc": "0220-3029", "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": "10 [hp_M]/10[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}