Package 44911-0388-1

Brand: lachesis

Generic: lachesis mutus
NDC Package

Package Facts

Identity

Package NDC 44911-0388-1
Digits Only 4491103881
Product NDC 44911-0388
Product ID 44911-0388_1bf41e20-8205-44f4-a88a-851b6c708db3
Description

30 mL in 1 BOTTLE, DROPPER (44911-0388-1)

Marketing

Marketing Status
Marketed Since 2016-08-22
Brand lachesis
Generic lachesis mutus
Sample Package No

Linked Drug Pages (1)

Lachesis ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1bf41e20-8205-44f4-a88a-851b6c708db3", "openfda": {"unii": ["VSW71SS07I"], "spl_set_id": ["25c87c59-6b32-494e-8c10-b34fa8bbd53d"], "manufacturer_name": ["Energique, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, DROPPER (44911-0388-1)", "package_ndc": "44911-0388-1", "marketing_start_date": "20160822"}], "brand_name": "Lachesis", "product_id": "44911-0388_1bf41e20-8205-44f4-a88a-851b6c708db3", "dosage_form": "LIQUID", "product_ndc": "44911-0388", "generic_name": "Lachesis Mutus", "labeler_name": "Energique, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lachesis", "active_ingredients": [{"name": "LACHESIS MUTA VENOM", "strength": "200 [hp_C]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20160822", "listing_expiration_date": "20261231"}