Package 69097-852-07
Brand: naproxen
Generic: naproxenPackage Facts
Identity
Package NDC
69097-852-07
Digits Only
6909785207
Product NDC
69097-852
Description
100 TABLET, DELAYED RELEASE in 1 BOTTLE (69097-852-07)
Marketing
Marketing Status
Brand
naproxen
Generic
naproxen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dcfba184-4397-4934-9392-2ac42f65e9e5", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0369097851071", "0369097852078"], "unii": ["57Y76R9ATQ"], "rxcui": ["311915", "603103"], "spl_set_id": ["e06c2b43-9882-442e-8413-10d9a33aecb9"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (69097-852-07)", "package_ndc": "69097-852-07", "marketing_start_date": "20160705"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (69097-852-12)", "package_ndc": "69097-852-12", "marketing_start_date": "20160705"}], "brand_name": "Naproxen", "product_id": "69097-852_dcfba184-4397-4934-9392-2ac42f65e9e5", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69097-852", "generic_name": "Naproxen", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "ANDA091432", "marketing_category": "ANDA", "marketing_start_date": "20160705", "listing_expiration_date": "20261231"}