Package 71205-747-00

Brand: diclofenac sodium

Generic: diclofenac sodium topical gel, 1%
NDC Package

Package Facts

Identity

Package NDC 71205-747-00
Digits Only 7120574700
Product NDC 71205-747
Description

1 TUBE in 1 CARTON (71205-747-00) / 100 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2023-01-18
Brand diclofenac sodium
Generic diclofenac sodium topical gel, 1%
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "b4694451-a13d-484e-92c4-c03a6fcbb511", "openfda": {"upc": ["0371205747008"], "unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["b4694451-a13d-484e-92c4-c03a6fcbb511"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (71205-747-00)  / 100 g in 1 TUBE", "package_ndc": "71205-747-00", "marketing_start_date": "20230118"}], "brand_name": "DICLOFENAC SODIUM", "product_id": "71205-747_b4694451-a13d-484e-92c4-c03a6fcbb511", "dosage_form": "GEL", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71205-747", "generic_name": "diclofenac sodium topical gel, 1%", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DICLOFENAC SODIUM", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "10 mg/g"}], "application_number": "ANDA210986", "marketing_category": "ANDA", "marketing_start_date": "20200914", "listing_expiration_date": "20261231"}