Package 0378-2150-01

Brand: meclofenamate sodium

Generic: meclofenamate sodium
NDC Package

Package Facts

Identity

Package NDC 0378-2150-01
Digits Only 0378215001
Product NDC 0378-2150
Product ID 0378-2150_26f16653-a1af-41b0-8152-6fb9faa96132
Description

100 CAPSULE in 1 BOTTLE, PLASTIC (0378-2150-01)

Marketing

Marketing Status
Marketed Since 1986-09-03
Brand meclofenamate sodium
Generic meclofenamate sodium
Sample Package No

Linked Drug Pages (1)

Meclofenamate Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "26f16653-a1af-41b0-8152-6fb9faa96132", "openfda": {"upc": ["0303783000015", "0303782150018"], "unii": ["94NJ818U2W"], "rxcui": ["618552", "618557"], "spl_set_id": ["96f19af4-de8f-4fd7-90d8-55fe6ebdd81d"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (0378-2150-01)", "package_ndc": "0378-2150-01", "marketing_start_date": "19860903"}], "brand_name": "Meclofenamate Sodium", "product_id": "0378-2150_26f16653-a1af-41b0-8152-6fb9faa96132", "dosage_form": "CAPSULE", "product_ndc": "0378-2150", "generic_name": "meclofenamate sodium", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclofenamate Sodium", "active_ingredients": [{"name": "MECLOFENAMATE SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA071081", "marketing_category": "ANDA", "marketing_start_date": "19860903", "listing_expiration_date": "20261231"}