Package 76420-012-30
Brand: diclofenac sodium
Generic: diclofenacPackage Facts
Identity
Package NDC
76420-012-30
Digits Only
7642001230
Product NDC
76420-012
Description
150 mL in 1 BOTTLE (76420-012-30)
Marketing
Marketing Status
Brand
diclofenac sodium
Generic
diclofenac
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "ead0dde9-f4f4-9f9b-e053-2a95a90ac6e5", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["857700"], "spl_set_id": ["9df599de-6412-a94e-e053-2995a90a1741"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "150 mL in 1 BOTTLE (76420-012-30)", "package_ndc": "76420-012-30", "marketing_start_date": "20200205"}], "brand_name": "Diclofenac Sodium", "product_id": "76420-012_ead0dde9-f4f4-9f9b-e053-2a95a90ac6e5", "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": "76420-012", "generic_name": "Diclofenac", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "16.05 mg/mL"}], "application_number": "ANDA206116", "marketing_category": "ANDA", "marketing_start_date": "20160902", "listing_expiration_date": "20261231"}