diclofenac sodium delayed release delayed release

Generic: diclofenac sodium

Labeler: cambridge therapeutics technologies, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac sodium delayed release delayed release
Generic Name diclofenac sodium
Labeler cambridge therapeutics technologies, llc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

diclofenac sodium 75 mg/1

Manufacturer
Cambridge Therapeutics Technologies, LLC

Identifiers & Regulatory

Product NDC 70882-128
Product ID 70882-128_b30b3f90-b9d8-4110-b0a8-5c18b8969832
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075185
Listing Expiration 2026-12-31
Marketing Start 1998-11-13

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] decreased prostaglandin production [pe] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70882128
Hyphenated Format 70882-128

Supplemental Identifiers

RxCUI
855926
UPC
0370882128308
UNII
QTG126297Q

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 delayed release (source: ndc)
Generic Name diclofenac sodium (source: ndc)
Application Number ANDA075185 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70882-128-30)
source: ndc

Packages (1)

70882-128-30 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70882-128-30)

Ingredients (1)

diclofenac sodium (75 mg/1)

Linked Drug Pages (1)

Diclofenac Sodium Delayed Release Delayed Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b30b3f90-b9d8-4110-b0a8-5c18b8969832", "openfda": {"upc": ["0370882128308"], "unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["fd544812-d7a9-47c8-9148-bea26c8b66c7"], "manufacturer_name": ["Cambridge Therapeutics Technologies, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70882-128-30)", "package_ndc": "70882-128-30", "marketing_start_date": "19981113"}], "brand_name": "Diclofenac Sodium Delayed Release Delayed Release", "product_id": "70882-128_b30b3f90-b9d8-4110-b0a8-5c18b8969832", "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": "70882-128", "generic_name": "Diclofenac Sodium", "labeler_name": "Cambridge Therapeutics Technologies, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium Delayed Release", "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"}