CEFPROZIL

Product NDC
52959-300
11-digit product format
529590300
Labeler code
52959
Product ID
52959-300_e39e2622-3fbf-474b-9c32-f052dc1a7eb2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CEFPROZIL
Dosage form
TABLET
Route
ORAL
Labeler
H. J. Harkins Company, Inc.
Application
ANDA065276
Marketing category
ANDA
Marketing start
2005-12-08
Marketing end
0000-00-00
Substance
CEFPROZIL
Active strength
500 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
228ef569-e7f1-4dcf-b820-c09522f86f2eProduct name120250129

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52959-300-202019-11-13C16284748780-197449f38-c76d-f6ea-e053-dbdaa90aa703CEFPROZIL TABLETS USP 250 mg and 500 mg Rx only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52959-300-20CEFPROZIL20 in 1 BOTTLETABLET203

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
52959-300-20EA - Each52959-300b1b833e2-c1df-47ef-8234-b490351fd2b712012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CEFPROZILACTIVE INGREDIENT4W0459ZA4VCEFPROZIL (CEFPROZIL) TABLET [H. J. HARKINS COMPANY, INC.]3
CEFPROZIL ANHYDROUSACTIVE MOIETY1M698F4H4ECEFPROZIL (CEFPROZIL) TABLET [H. J. HARKINS COMPANY, INC.]3
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCEFPROZIL (CEFPROZIL) TABLET [H. J. HARKINS COMPANY, INC.]3
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CEFPROZIL (CEFPROZIL) TABLET [H. J. HARKINS COMPANY, INC.]3
METHYLCELLULOSE (15 CPS)INACTIVE INGREDIENTNPU9M2E6L8CEFPROZIL (CEFPROZIL) TABLET [H. J. HARKINS COMPANY, INC.]3
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2CEFPROZIL (CEFPROZIL) TABLET [H. J. HARKINS COMPANY, INC.]3
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPCEFPROZIL (CEFPROZIL) TABLET [H. J. HARKINS COMPANY, INC.]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52959-300CEFPROZIL (CEFPROZIL) TABLET [H. J. HARKINS COMPANY, INC.]3Legacy NDC, 1 package rows20111116_17a1975e-ce3b-4057-ae5b-8d191319caa7.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197453cefprozil 500 MG Oral TabletPSN17a1975e-ce3b-4057-ae5b-8d191319caa73
197453cefprozil 500 MG Oral TabletSCD17a1975e-ce3b-4057-ae5b-8d191319caa73

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
52959-300-205295903002020 in 1 BOTTLEHistorical