Package 76472-3022-1

Brand: lachesis mutus 200ck

Generic: lachesis mutus
NDC Package

Package Facts

Identity

Package NDC 76472-3022-1
Digits Only 7647230221
Product NDC 76472-3022
Description

80 PELLET in 1 CYLINDER (76472-3022-1)

Marketing

Marketing Status
Marketed Since 2011-11-23
Brand lachesis mutus 200ck
Generic lachesis mutus
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBLINGUAL"], "spl_id": "35b7588a-3001-1ce7-e063-6394a90ab714", "openfda": {"unii": ["VSW71SS07I"], "spl_set_id": ["cf85728d-07c8-5a23-e053-2995a90aa6cd"], "manufacturer_name": ["SEVENE USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 PELLET in 1 CYLINDER (76472-3022-1)", "package_ndc": "76472-3022-1", "marketing_start_date": "20111123"}], "brand_name": "LACHESIS MUTUS 200ck", "product_id": "76472-3022_35b7588a-3001-1ce7-e063-6394a90ab714", "dosage_form": "PELLET", "product_ndc": "76472-3022", "generic_name": "LACHESIS MUTUS", "labeler_name": "SEVENE USA", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LACHESIS MUTUS", "brand_name_suffix": "200ck", "active_ingredients": [{"name": "LACHESIS MUTA VENOM", "strength": "200 [kp_C]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20111123", "listing_expiration_date": "20261231"}