Home NDC 65697-450 NDC 65697-450 - Clanza CR This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 65697-450
Package NDCs from labels 65697-450-20, 65697-450-21, 65697-450-22
Manufacturer United Douglas Pharm., Inc. | Korea United Pharm Inc.
Effective date 2011-11-02
Current FDA listing Not matched in FDA.report NDC product tables FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 65697-450-20 ClanzaCR 1 in 1 PACKET TABLET, FILM COATED 1 7 65697-450-21 ClanzaCR 10 in 1 BLISTER PACK TABLET, FILM COATED 10 7 65697-450-22 ClanzaCR 10 in 1 CARTON TABLET, FILM COATED 10 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 65697-450 CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 3 package rows 20111103_8a023942-01e8-4849-aa3c-1a640ffc7fd3.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Aceclofenac ACTIVE INGREDIENT RPK779R03H CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Aceclofenac ACTIVE MOIETY RPK779R03H CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Alcohol INACTIVE INGREDIENT 3K9958V90M CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Carbomer 941 INACTIVE INGREDIENT F68VH75CJC CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Cellulose, Microcrystalline INACTIVE INGREDIENT OP1R32D61U CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Colloidal Silicon Dioxide INACTIVE INGREDIENT ETJ7Z6XBU4 CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Crospovidone INACTIVE INGREDIENT 68401960MK CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Diethyl Phthalate INACTIVE INGREDIENT UF064M00AF CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Ethylcelluloses INACTIVE INGREDIENT 7Z8S9VYZ4B CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Hypromellose 2208 (15000 MPA.S) INACTIVE INGREDIENT Z78RG6M2N2 CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Hypromellose 2910 (5 MPA.S) INACTIVE INGREDIENT R75537T0T4 CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Hypromellose 2910 (6 MPA.S) INACTIVE INGREDIENT 0WZ8WG20P6 CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Lactose Monohydrate INACTIVE INGREDIENT EWQ57Q8I5X CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Magnesium Stearate INACTIVE INGREDIENT 70097M6I30 CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Methylene Chloride INACTIVE INGREDIENT 588X2YUY0A CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Poloxamer 407 INACTIVE INGREDIENT TUF2IVW3M2 CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Sodium Carbonate INACTIVE INGREDIENT 45P3261C7T CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7 Titanium Dioxide INACTIVE INGREDIENT 15FIX9V2JP CLANZA CR (ACECLOFENAC) TABLET, FILM COATED [UNITED DOUGLAS PHARM., INC.] 7
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 191 of 271 · 5,410 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Anti Bacterial Hand Gel Frozen Lake ALCOHOL Bath & Body Works, Inc. 29a536d5-6abb-c0ef-e063-6394a90a15bb 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Marshmallow Pumpkin Latte ALCOHOL Bath & Body Works, Inc. 29a5342a-e6dc-ea55-e063-6394a90a11e8 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pumpkin Apple ALCOHOL Bath & Body Works, Inc. 29a536d5-6abf-c0ef-e063-6394a90a15bb 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Rainfall ALCOHOL Bath & Body Works, Inc. 29a54361-e107-20d7-e063-6294a90a117a 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pumpkin Cupcake ALCOHOL Bath & Body Works, Inc. 29a53c91-0bda-f572-e063-6294a90ae895 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sweater Weather ALCOHOL Bath & Body Works, Inc. 29a540fd-60b7-eb1e-e063-6394a90a27f7 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Alcohol Antiseptic 70% Topical Solution ALCOHOL Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc aa95e99f-5c17-c394-e053-2995a90a6bf9 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Thick Hand Sanitizer ALCOHOL Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc a35b4c26-469b-72ec-e053-2a95a90a0510 2024-12-19 Warnings Exact identifier unii: 3K9958V90M germstarONE unscented ETHYL ALCOHOL Soaptronic, LLC a6a798bd-09cb-1853-e053-2995a90a27f9 2024-12-19 Warnings Exact identifier unii: 3K9958V90M EXTENDED CARE Foaming Hand Sanitizer ALCOHOL TRIPLE A SUPPLIES, INC. f244f9c0-82c6-42a8-b0a8-63af546ed26f 2024-12-19 Warnings Exact identifier unii: 3K9958V90M germstarCitrus ETHYL ALCOHOL Soaptronic, LLC 779abef7-53ff-47c3-b7e6-27570eb055b3 2024-12-19 Warnings Exact identifier unii: 3K9958V90M germstarGel ETHYL ALCOHOL Soaptronic, LLC b5fd6c3c-d452-74e6-e053-2995a90a9090 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Cucumber Melon ALCOHOL Bath & Body Works, Inc. 29a63c54-116f-30bb-e063-6394a90a8c6f 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Frosted Coconut Snowball ALCOHOL Bath & Body Works, Inc. 29a652a8-15fd-80d4-e063-6394a90acb4d 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Black Cherry Frost ALCOHOL Bath & Body Works, Inc. 29a654df-016b-830e-e063-6394a90a1062 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Winterberry Ice ALCOHOL Bath & Body Works, Inc. 29a64c95-eb54-8081-e063-6394a90a0726 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Magic In The Air ALCOHOL Bath & Body Works, Inc. 29a651e4-a014-57d2-e063-6394a90a35f0 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sweet Tea and Lemonade ALCOHOL Bath & Body Works, Inc. 29a64de5-af39-5a91-e063-6394a90ac35c 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Honolulu Sun ALCOHOL Bath & Body Works, Inc. 29a64c62-8517-1b39-e063-6294a90a35a8 2024-12-19 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Strawberry Snowflakes ALCOHOL Bath & Body Works, Inc. 29a651e4-a016-57d2-e063-6394a90a35f0 2024-12-19 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.