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
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Matched openFDA labels page 210 of 271 · 5,408 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.