Package 76282-103-39

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 76282-103-39
Digits Only 7628210339
Product NDC 76282-103
Description

1 TUBE in 1 CARTON (76282-103-39) / 100 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2024-07-30
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": "6fc74e92-7f37-41e7-aa8b-8fd0275a57c9", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["be25c19e-cbea-4f87-a581-9f0d350e5adf"], "manufacturer_name": ["EXELAN PHARMACEUTICALS INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (76282-103-39)  / 100 g in 1 TUBE", "package_ndc": "76282-103-39", "marketing_start_date": "20240730"}], "brand_name": "Diclofenac Sodium", "product_id": "76282-103_6fc74e92-7f37-41e7-aa8b-8fd0275a57c9", "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": "76282-103", "generic_name": "Diclofenac sodium", "labeler_name": "EXELAN PHARMACEUTICALS INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "10 mg/g"}], "application_number": "ANDA209903", "marketing_category": "ANDA", "marketing_start_date": "20240730", "listing_expiration_date": "20261231"}