Package 67296-2155-1

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 67296-2155-1
Digits Only 6729621551
Product NDC 67296-2155
Description

1 TUBE in 1 CARTON (67296-2155-1) / 100 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2023-05-10
Brand diclofenac sodium
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "45d26c5e-9537-0ade-e063-6394a90afb9a", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["37362eb4-db16-f4ad-e063-6394a90a42aa"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (67296-2155-1)  / 100 g in 1 TUBE", "package_ndc": "67296-2155-1", "marketing_start_date": "20230510"}], "brand_name": "Diclofenac Sodium", "product_id": "67296-2155_45d26c5e-9537-0ade-e063-6394a90afb9a", "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": "67296-2155", "generic_name": "Diclofenac Sodium", "labeler_name": "Redpharm Drug", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "10 mg/g"}], "application_number": "ANDA204306", "marketing_category": "ANDA", "marketing_start_date": "20230510", "listing_expiration_date": "20261231"}