Package 0220-0164-41

Brand: alfalfa

Generic: alfalfa
NDC Package

Package Facts

Identity

Package NDC 0220-0164-41
Digits Only 0220016441
Product NDC 0220-0164
Description

6 [hp_X] in 1 TUBE (0220-0164-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand alfalfa
Generic alfalfa
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "079c8b50-d1d8-a2a2-e063-6294a90a7a60", "openfda": {"unii": ["DJO934BRBD"], "spl_set_id": ["87338363-7f5f-6a2e-e053-2a91aa0ab508"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_X] in 1 TUBE (0220-0164-41)", "package_ndc": "0220-0164-41", "marketing_start_date": "19830303"}], "brand_name": "Alfalfa", "product_id": "0220-0164_079c8b50-d1d8-a2a2-e063-6294a90a7a60", "dosage_form": "PELLET", "product_ndc": "0220-0164", "generic_name": "ALFALFA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alfalfa", "active_ingredients": [{"name": "ALFALFA", "strength": "6 [hp_X]/6[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}