Package 51672-1358-2
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
51672-1358-2
Digits Only
5167213582
Product NDC
51672-1358
Description
1 BOTTLE, DROPPER in 1 CARTON (51672-1358-2) / 150 mL in 1 BOTTLE, DROPPER
Marketing
Marketing Status
Brand
diclofenac sodium
Generic
diclofenac sodium
Sample Package
No
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4b20d36c-e921-489d-e063-6294a90ad63b", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["857700"], "spl_set_id": ["fae53d24-acf1-4250-888d-b8d965ffc3d3"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (51672-1358-2) / 150 mL in 1 BOTTLE, DROPPER", "package_ndc": "51672-1358-2", "marketing_start_date": "20141126"}], "brand_name": "Diclofenac Sodium", "product_id": "51672-1358_4b20d36c-e921-489d-e063-6294a90ad63b", "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": "51672-1358", "generic_name": "Diclofenac Sodium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "16.05 mg/mL"}], "application_number": "ANDA203818", "marketing_category": "ANDA", "marketing_start_date": "20141126", "listing_expiration_date": "20271231"}