Package 60760-190-30

Brand: naproxen

Generic: naproxen
NDC Package

Package Facts

Identity

Package NDC 60760-190-30
Digits Only 6076019030
Product NDC 60760-190
Description

30 TABLET in 1 BOTTLE, PLASTIC (60760-190-30)

Marketing

Marketing Status
Marketed Since 2017-11-10
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": "29171c9a-0bd4-435f-e063-6394a90ad7c9", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ"], "rxcui": ["198014"], "spl_set_id": ["5de3af7c-2c77-6b04-e053-2991aa0ae3fa"], "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": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (60760-190-14)", "package_ndc": "60760-190-14", "marketing_start_date": "20180305"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (60760-190-15)", "package_ndc": "60760-190-15", "marketing_start_date": "20171110"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (60760-190-20)", "package_ndc": "60760-190-20", "marketing_start_date": "20171110"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-190-30)", "package_ndc": "60760-190-30", "marketing_start_date": "20171110"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-190-60)", "package_ndc": "60760-190-60", "marketing_start_date": "20171110"}], "brand_name": "Naproxen", "product_id": "60760-190_29171c9a-0bd4-435f-e063-6394a90ad7c9", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "60760-190", "generic_name": "Naproxen", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "ANDA078250", "marketing_category": "ANDA", "marketing_start_date": "20070701", "listing_expiration_date": "20261231"}