Package 0220-2940-41

Brand: kreosotum

Generic: wood creosote
NDC Package

Package Facts

Identity

Package NDC 0220-2940-41
Digits Only 0220294041
Product NDC 0220-2940
Description

1 [hp_M] in 1 TUBE (0220-2940-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand kreosotum
Generic wood creosote
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0e390d-fe5e-9dc6-e063-6294a90a5f58", "openfda": {"unii": ["3JYG22FD73"], "spl_set_id": ["8619e4e5-0c55-45db-e053-2a91aa0aa6b7"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 [hp_M] in 1 TUBE (0220-2940-41)", "package_ndc": "0220-2940-41", "marketing_start_date": "19830303"}], "brand_name": "Kreosotum", "product_id": "0220-2940_0a0e390d-fe5e-9dc6-e063-6294a90a5f58", "dosage_form": "PELLET", "product_ndc": "0220-2940", "generic_name": "WOOD CREOSOTE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kreosotum", "active_ingredients": [{"name": "WOOD CREOSOTE", "strength": "1 [hp_M]/[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}