Package 68788-8237-1

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 68788-8237-1
Digits Only 6878882371
Product NDC 68788-8237
Product ID 68788-8237_488f67d7-bbdd-44fd-bd37-20ce051d5970
Description

1 TUBE in 1 CARTON (68788-8237-1) / 100 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2022-08-09
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": ["TOPICAL"], "spl_id": "488f67d7-bbdd-44fd-bd37-20ce051d5970", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["632f553b-130a-4d45-8dcd-fe6fcf6a9ab8"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68788-8237-1)  / 100 g in 1 TUBE", "package_ndc": "68788-8237-1", "marketing_start_date": "20220809"}], "brand_name": "diclofenac sodium", "product_id": "68788-8237_488f67d7-bbdd-44fd-bd37-20ce051d5970", "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": "68788-8237", "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": "30 mg/g"}], "application_number": "ANDA210893", "marketing_category": "ANDA", "marketing_start_date": "20220809", "listing_expiration_date": "20261231"}