Package 0220-3642-41

Brand: natrum sulphuricum

Generic: sodium sulfate
NDC Package

Package Facts

Identity

Package NDC 0220-3642-41
Digits Only 0220364241
Product NDC 0220-3642
Description

200 [kp_C] in 1 TUBE (0220-3642-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
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": "f2f67abe-f21b-a19e-e053-2995a90a6b3f", "openfda": {"unii": ["0YPR65R21J"], "spl_set_id": ["86560034-d62b-57d3-e053-2991aa0a7f13"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-3642-41)", "package_ndc": "0220-3642-41", "marketing_start_date": "19830303"}], "brand_name": "Natrum sulphuricum", "product_id": "0220-3642_f2f67abe-f21b-a19e-e053-2995a90a6b3f", "dosage_form": "PELLET", "product_ndc": "0220-3642", "generic_name": "SODIUM SULFATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Natrum sulphuricum", "active_ingredients": [{"name": "SODIUM SULFATE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}