diclofenac sodium delayed release
Generic: diclofenac sodium
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
diclofenac sodium delayed release
Generic Name
diclofenac sodium
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
diclofenac sodium 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8952
Product ID
68788-8952_bef4d22d-6e29-46ed-bb04-55b1b18e7f20
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075185
Listing Expiration
2026-12-31
Marketing Start
2015-11-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888952
Hyphenated Format
68788-8952
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
diclofenac sodium delayed release (source: ndc)
Generic Name
diclofenac sodium (source: ndc)
Application Number
ANDA075185 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-1)
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-3)
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-6)
- 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-8)
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-9)
Packages (5)
68788-8952-1
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-1)
68788-8952-3
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-3)
68788-8952-6
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-6)
68788-8952-8
120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-8)
68788-8952-9
90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bef4d22d-6e29-46ed-bb04-55b1b18e7f20", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["e947653c-6789-4c15-82c9-4b1402f6d6ac"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-1)", "package_ndc": "68788-8952-1", "marketing_start_date": "20151120"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-3)", "package_ndc": "68788-8952-3", "marketing_start_date": "20151120"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-6)", "package_ndc": "68788-8952-6", "marketing_start_date": "20151120"}, {"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-8)", "package_ndc": "68788-8952-8", "marketing_start_date": "20151120"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-9)", "package_ndc": "68788-8952-9", "marketing_start_date": "20151120"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "68788-8952_bef4d22d-6e29-46ed-bb04-55b1b18e7f20", "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": "68788-8952", "generic_name": "Diclofenac Sodium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "brand_name_suffix": "Delayed Release", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "20151120", "listing_expiration_date": "20261231"}