Package 76420-042-14

Brand: naproxen

Generic: naproxen
NDC Package

Package Facts

Identity

Package NDC 76420-042-14
Digits Only 7642004214
Product NDC 76420-042
Description

14 TABLET in 1 BOTTLE, PLASTIC (76420-042-14)

Marketing

Marketing Status
Marketed Since 2020-02-05
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": "ead160e6-aba4-ca0a-e053-2a95a90ab964", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ"], "rxcui": ["198014"], "spl_set_id": ["a4fcb411-c918-459b-adc6-06dfa8ed8a50"], "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": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET in 1 BOTTLE, PLASTIC (76420-042-01)", "package_ndc": "76420-042-01", "marketing_start_date": "20200205"}, {"sample": false, "description": "2 TABLET in 1 BOTTLE, PLASTIC (76420-042-02)", "package_ndc": "76420-042-02", "marketing_start_date": "20200205"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (76420-042-10)", "package_ndc": "76420-042-10", "marketing_start_date": "20200205"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (76420-042-14)", "package_ndc": "76420-042-14", "marketing_start_date": "20200205"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (76420-042-30)", "package_ndc": "76420-042-30", "marketing_start_date": "20200205"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (76420-042-60)", "package_ndc": "76420-042-60", "marketing_start_date": "20200205"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (76420-042-90)", "package_ndc": "76420-042-90", "marketing_start_date": "20200205"}], "brand_name": "NAPROXEN", "product_id": "76420-042_ead160e6-aba4-ca0a-e053-2a95a90ab964", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "76420-042", "generic_name": "NAPROXEN", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NAPROXEN", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "ANDA091416", "marketing_category": "ANDA", "marketing_start_date": "20160706", "listing_expiration_date": "20261231"}