Package 0220-3131-41

Brand: lithium carbonicum

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 0220-3131-41
Digits Only 0220313141
Product NDC 0220-3131
Description

30 [hp_C] in 1 TUBE (0220-3131-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand lithium carbonicum
Generic lithium carbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0e6def-a7b5-d1cc-e063-6294a90a317b", "openfda": {"unii": ["2BMD2GNA4V"], "spl_set_id": ["68f8e2a1-0fe9-70e4-e053-2a91aa0a981d"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-3131-41)", "package_ndc": "0220-3131-41", "marketing_start_date": "19830303"}], "brand_name": "Lithium carbonicum", "product_id": "0220-3131_0a0e6def-a7b5-d1cc-e063-6294a90a317b", "dosage_form": "PELLET", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "0220-3131", "generic_name": "LITHIUM CARBONATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lithium carbonicum", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}