Package 71205-450-15
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
71205-450-15
Digits Only
7120545015
Product NDC
71205-450
Description
1 BOTTLE in 1 CARTON (71205-450-15) / 150 mL in 1 BOTTLE
Marketing
Marketing Status
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": "7bc185e2-e749-4a24-8550-c2f6d39222d2", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["857700"], "spl_set_id": ["7bc185e2-e749-4a24-8550-c2f6d39222d2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (71205-450-15) / 150 mL in 1 BOTTLE", "package_ndc": "71205-450-15", "marketing_start_date": "20200421"}], "brand_name": "Diclofenac Sodium", "product_id": "71205-450_7bc185e2-e749-4a24-8550-c2f6d39222d2", "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": "71205-450", "generic_name": "diclofenac sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "16.05 mg/mL"}], "application_number": "ANDA202769", "marketing_category": "ANDA", "marketing_start_date": "20180731", "listing_expiration_date": "20261231"}