Package 70518-2345-2
Brand: lithium carbonate
Generic: lithium carbonatePackage Facts
Identity
Package NDC
70518-2345-2
Digits Only
7051823452
Product NDC
70518-2345
Description
30 CAPSULE, GELATIN COATED in 1 BLISTER PACK (70518-2345-2)
Marketing
Marketing Status
Brand
lithium carbonate
Generic
lithium carbonate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a03bc22-bc9a-028d-e063-6294a90a8e7b", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197893"], "spl_set_id": ["b074ca9f-66b2-4e83-b67d-cb317b46411b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, GELATIN COATED in 1 BLISTER PACK (70518-2345-2)", "package_ndc": "70518-2345-2", "marketing_start_date": "20221111"}], "brand_name": "Lithium Carbonate", "product_id": "70518-2345_4a03bc22-bc9a-028d-e063-6294a90a8e7b", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "70518-2345", "generic_name": "Lithium Carbonate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "600 mg/1"}], "application_number": "NDA017812", "marketing_category": "NDA", "marketing_start_date": "20191004", "listing_expiration_date": "20271231"}