Package 60687-806-01

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 60687-806-01
Digits Only 6068780601
Product NDC 60687-806
Description

100 BLISTER PACK in 1 CARTON (60687-806-01) / 1 CAPSULE in 1 BLISTER PACK (60687-806-11)

Marketing

Marketing Status
Marketed Since 2024-06-16
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": "4b477af8-c21c-6d93-e063-6394a90abaa1", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197889"], "spl_set_id": ["049902a9-3af1-4863-994e-15f36e7a9793"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-806-01)  / 1 CAPSULE in 1 BLISTER PACK (60687-806-11)", "package_ndc": "60687-806-01", "marketing_start_date": "20240616"}], "brand_name": "Lithium Carbonate", "product_id": "60687-806_4b477af8-c21c-6d93-e063-6394a90abaa1", "dosage_form": "CAPSULE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "60687-806", "generic_name": "Lithium Carbonate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA079139", "marketing_category": "ANDA", "marketing_start_date": "20240616", "listing_expiration_date": "20271231"}