Package 0220-3128-41

Brand: lithium carbonicum

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 0220-3128-41
Digits Only 0220312841
Product NDC 0220-3128
Product ID 0220-3128_0a0e6b08-3f35-b3f7-e063-6394a90ae8e3
Description

200 [kp_C] in 1 TUBE (0220-3128-41)

Marketing

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

Linked Drug Pages (1)

Lithium carbonicum ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a0e6b08-3f35-b3f7-e063-6394a90ae8e3", "openfda": {"unii": ["2BMD2GNA4V"], "spl_set_id": ["861df6e6-46cb-632d-e053-2a91aa0ae9a3"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-3128-41)", "package_ndc": "0220-3128-41", "marketing_start_date": "19830303"}], "brand_name": "Lithium carbonicum", "product_id": "0220-3128_0a0e6b08-3f35-b3f7-e063-6394a90ae8e3", "dosage_form": "PELLET", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "0220-3128", "generic_name": "LITHIUM CARBONATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lithium carbonicum", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}