CEFPROZIL

Product NDC
68180-403
11-digit product format
681800403
Labeler code
68180
Product ID
68180-403_b5bc3f77-ca01-4c3f-b8b6-591a3d8f73f4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CEFPROZIL
Dosage form
TABLET
Route
ORAL
Labeler
Lupin Pharmaceuticals, Inc.
Application
ANDA065276
Marketing category
ANDA
Marketing start
2005-12-01
Substance
CEFPROZIL
Active strength
250 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
CEFPROZIL
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CEFPROZIL250 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4W0459ZA4V
Rxcui197452, 197453

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68180-403-01CEFPROZIL100 in 1 BOTTLETABLET10010

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68180-403-01EA - Each68180-4035df7ec43-91ef-461e-a3ee-8f8ccf781cec12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CEFPROZILACTIVE INGREDIENT4W0459ZA4VCEFPROZIL TABLET [LUPIN PHARMACEUTICALS, INC.]3
CEFPROZIL ANHYDROUSACTIVE MOIETY1M698F4H4ECEFPROZIL TABLET [LUPIN PHARMACEUTICALS, INC.]3
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCEFPROZIL TABLET [LUPIN PHARMACEUTICALS, INC.]3
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8CEFPROZIL TABLET [LUPIN PHARMACEUTICALS, INC.]3
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CEFPROZIL TABLET [LUPIN PHARMACEUTICALS, INC.]3
METHYLCELLULOSE (15 CPS)INACTIVE INGREDIENTNPU9M2E6L8CEFPROZIL TABLET [LUPIN PHARMACEUTICALS, INC.]3
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2CEFPROZIL TABLET [LUPIN PHARMACEUTICALS, INC.]3
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPCEFPROZIL TABLET [LUPIN PHARMACEUTICALS, INC.]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68180-403CEFPROZIL TABLET [LUPIN PHARMACEUTICALS, INC.]9Current NDC, Legacy NDC, 1 package rows20250130_14527f4a-ce99-449d-a5a5-9edd7fb28dee.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197452cefprozil 250 MG Oral TabletPSN14527f4a-ce99-449d-a5a5-9edd7fb28dee10
197453cefprozil 500 MG Oral TabletPSN14527f4a-ce99-449d-a5a5-9edd7fb28dee10
197452cefprozil 250 MG Oral TabletSCD14527f4a-ce99-449d-a5a5-9edd7fb28dee10
197453cefprozil 500 MG Oral TabletSCD14527f4a-ce99-449d-a5a5-9edd7fb28dee10

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68180-403-0168180040301100 TABLET in 1 BOTTLE (68180-403-01) 100 tablet2005-12-010000-00-00NoNoCurrent