Package 0220-3639-41

Brand: natrum sulphuricum

Generic: sodium sulfate
NDC Package

Package Facts

Identity

Package NDC 0220-3639-41
Digits Only 0220363941
Product NDC 0220-3639
Description

30 [hp_C] in 1 TUBE (0220-3639-41)

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": "f913e22d-1f2f-b142-e053-6394a90a1659", "openfda": {"unii": ["0YPR65R21J"], "spl_set_id": ["8655cd7d-aa97-ec6f-e053-2a91aa0a33db"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-3639-41)", "package_ndc": "0220-3639-41", "marketing_start_date": "19830303"}], "brand_name": "Natrum sulphuricum", "product_id": "0220-3639_f913e22d-1f2f-b142-e053-6394a90a1659", "dosage_form": "PELLET", "product_ndc": "0220-3639", "generic_name": "SODIUM SULFATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Natrum sulphuricum", "active_ingredients": [{"name": "SODIUM SULFATE", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}