Package 0220-3842-41

Brand: oxalicum acidum

Generic: oxalic acid dihydrate
NDC Package

Package Facts

Identity

Package NDC 0220-3842-41
Digits Only 0220384241
Product NDC 0220-3842
Description

30 [hp_C] in 1 TUBE (0220-3842-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand oxalicum acidum
Generic oxalic acid dihydrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a211521-c517-7c84-e063-6294a90a0a8a", "openfda": {"unii": ["0K2L2IJ59O"], "spl_set_id": ["865b4812-11df-8ee8-e053-2a91aa0ad4c5"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-3842-41)", "package_ndc": "0220-3842-41", "marketing_start_date": "19830303"}], "brand_name": "Oxalicum acidum", "product_id": "0220-3842_0a211521-c517-7c84-e063-6294a90a0a8a", "dosage_form": "PELLET", "product_ndc": "0220-3842", "generic_name": "OXALIC ACID DIHYDRATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Oxalicum acidum", "active_ingredients": [{"name": "OXALIC ACID DIHYDRATE", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}