Package 0378-2086-77

Brand: dexlansoprazole

Generic: dexlansoprazole
NDC Package

Package Facts

Identity

Package NDC 0378-2086-77
Digits Only 0378208677
Product NDC 0378-2086
Product ID 0378-2086_bd08545b-3f1d-44c5-bdd9-05acd7f69a0a
Description

90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-2086-77)

Marketing

Marketing Status
Marketed Since 2024-01-22
Brand dexlansoprazole
Generic dexlansoprazole
Sample Package No

Linked Drug Pages (1)

Dexlansoprazole ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bd08545b-3f1d-44c5-bdd9-05acd7f69a0a", "openfda": {"upc": ["0303782086935", "0303782085938"], "unii": ["HS2S9VK3NH"], "rxcui": ["833204", "833213"], "spl_set_id": ["3f9699b5-7614-41cb-bd1d-ff02930e98f3"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-2086-77)", "package_ndc": "0378-2086-77", "marketing_start_date": "20240122"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-2086-93)", "package_ndc": "0378-2086-93", "marketing_start_date": "20240122"}], "brand_name": "Dexlansoprazole", "product_id": "0378-2086_bd08545b-3f1d-44c5-bdd9-05acd7f69a0a", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0378-2086", "generic_name": "dexlansoprazole", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexlansoprazole", "active_ingredients": [{"name": "DEXLANSOPRAZOLE SESQUIHYDRATE", "strength": "60 mg/1"}], "application_number": "ANDA205205", "marketing_category": "ANDA", "marketing_start_date": "20240122", "listing_expiration_date": "20261231"}