Package 76420-134-05

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 76420-134-05
Digits Only 7642013405
Product NDC 76420-134
Product ID 76420-134_b965985a-9568-58f3-e053-2995a90a008c
Description

150 mL in 1 BOTTLE (76420-134-05)

Marketing

Marketing Status
Marketed Since 2021-01-21
Brand diclofenac sodium
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (1)

Diclofenac Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TRANSDERMAL"], "spl_id": "b965985a-9568-58f3-e053-2995a90a008c", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["857700"], "spl_set_id": ["f3f60cd3-8f1f-4ca4-9621-805b4a6c35a8"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "150 mL in 1 BOTTLE (76420-134-05)", "package_ndc": "76420-134-05", "marketing_start_date": "20210121"}], "brand_name": "Diclofenac Sodium", "product_id": "76420-134_b965985a-9568-58f3-e053-2995a90a008c", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "76420-134", "generic_name": "Diclofenac Sodium", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "16.05 mg/mL"}], "application_number": "ANDA204132", "marketing_category": "ANDA", "marketing_start_date": "20150820", "listing_expiration_date": "20261231"}