Package 0378-6688-77

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 0378-6688-77
Digits Only 0378668877
Product NDC 0378-6688
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-6688-77)

Marketing

Marketing Status
Marketed Since 2011-01-19
Brand pantoprazole sodium
Generic pantoprazole sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38896560-f523-4d0b-8113-5ff7f5f38c81", "openfda": {"upc": ["0303786689774", "0303786688777"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["56ad5b97-8e5f-48a5-b2ba-a5484b43d018"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-6688-77)", "package_ndc": "0378-6688-77", "marketing_start_date": "20110119"}], "brand_name": "Pantoprazole Sodium", "product_id": "0378-6688_38896560-f523-4d0b-8113-5ff7f5f38c81", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0378-6688", "generic_name": "pantoprazole sodium", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA090970", "marketing_category": "ANDA", "marketing_start_date": "20110119", "listing_expiration_date": "20261231"}