Package 68788-8541-1

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 68788-8541-1
Digits Only 6878885411
Product NDC 68788-8541
Description

1 BOTTLE in 1 CARTON (68788-8541-1) / 112 g in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-10-25
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": "d649db54-e6e3-4e3b-83df-b73dc31fabe0", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["1487074"], "spl_set_id": ["15b280a1-4964-4636-833b-3db44044d289"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68788-8541-1)  / 112 g in 1 BOTTLE", "package_ndc": "68788-8541-1", "marketing_start_date": "20231025"}], "brand_name": "Diclofenac Sodium", "product_id": "68788-8541_d649db54-e6e3-4e3b-83df-b73dc31fabe0", "dosage_form": "SOLUTION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-8541", "generic_name": "Diclofenac Sodium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "20 mg/g"}], "application_number": "ANDA213040", "marketing_category": "ANDA", "marketing_start_date": "20231025", "listing_expiration_date": "20261231"}