Package 68071-4934-4

Brand: diclofenac sodium delayed release

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 68071-4934-4
Digits Only 6807149344
Product NDC 68071-4934
Description

14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4934-4)

Marketing

Marketing Status
Marketed Since 2019-06-21
Brand diclofenac sodium delayed release
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1ae26991-057e-97d4-e063-6294a90adc65", "openfda": {"upc": ["0368071493443"], "unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["8bda6135-c957-6b4e-e053-2995a90a0cb5"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4934-4)", "package_ndc": "68071-4934-4", "marketing_start_date": "20190621"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "68071-4934_1ae26991-057e-97d4-e063-6294a90adc65", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-4934", "generic_name": "Diclofenac Sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "brand_name_suffix": "Delayed Release", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "19981113", "listing_expiration_date": "20261231"}