Package 0220-3643-41
Brand: natrum sulphuricum
Generic: sodium sulfatePackage Facts
Identity
Package NDC
0220-3643-41
Digits Only
0220364341
Product NDC
0220-3643
Description
1 [hp_M] in 1 TUBE (0220-3643-41)
Marketing
Marketing Status
Brand
natrum sulphuricum
Generic
sodium sulfate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a1fbdfd-54f3-cbfd-e063-6394a90a2db8", "openfda": {"unii": ["0YPR65R21J"], "spl_set_id": ["86564f9d-36b5-39cb-e053-2991aa0a5007"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 [hp_M] in 1 TUBE (0220-3643-41)", "package_ndc": "0220-3643-41", "marketing_start_date": "19830303"}], "brand_name": "Natrum sulphuricum", "product_id": "0220-3643_0a1fbdfd-54f3-cbfd-e063-6394a90a2db8", "dosage_form": "PELLET", "product_ndc": "0220-3643", "generic_name": "SODIUM SULFATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Natrum sulphuricum", "active_ingredients": [{"name": "SODIUM SULFATE", "strength": "1 [hp_M]/[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}