Nifedical

Product NDC
53808-0851
11-digit product format
538080851
Labeler code
53808
Product ID
53808-0851_543b34f9-d0d4-47bb-ad9a-b3b7eaec442e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
nifedipine
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
State of Florida DOH Central Pharmacy
Application
ANDA075289
Marketing category
ANDA
Marketing start
2013-01-01
Marketing end
0000-00-00
Substance
NIFEDIPINE
Active strength
60 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bbd94e90-e531-9113-45c1-29860f331640Product name720230104
5e4d0a9b-8ce4-418c-bf0c-d2b4be281ffdProduct name420220126
308fd2ea-d88a-e021-96c1-7c2ab74d6e4bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53808-0851-12020-01-31C16284748780-19d75b9cf-f776-f424-e053-dadaa90a57ceNifedical XL ® (NIFEDIPINE) Tablet, Film Coated Extended Release USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53808-0851-1NifedicalXL30 in 1 BLISTER PACKTABLET, FILM COATED, EXTENDED RE301

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
NIFEDIPINEACTIVE INGREDIENTI9ZF7L6G2LNIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
NIFEDIPINEACTIVE MOIETYI9ZF7L6G2LNIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
ANHYDROUS LACTOSEINACTIVE INGREDIENT3SY5LH9PMKNIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UNIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
COLLOIDAL SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4NIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
ETHYLCELLULOSESINACTIVE INGREDIENT7Z8S9VYZ4BNIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675NIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)INACTIVE INGREDIENTS38J6RZN16NIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WONIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30NIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)INACTIVE INGREDIENT74G4R6TH13NIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:2)INACTIVE INGREDIENT5KY68S2577NIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1ANIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JNIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
TALCINACTIVE INGREDIENT7SEV7J4R1UNIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPNIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53808-0851NIFEDICAL XL (NIFEDIPINE) TABLET, FILM COATED, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]1Legacy NDC, 1 package rows20140415_8c5b2ff0-fd2b-4915-a14c-e18ab0bdf018.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
351438Nifedical XL 60 MG 24HR Extended Release Oral TabletPSN8c5b2ff0-fd2b-4915-a14c-e18ab0bdf0181
1812013NIFEdipine 60 MG Osmotic 24HR Extended Release Oral TabletPSN8c5b2ff0-fd2b-4915-a14c-e18ab0bdf0181
351438Osmotic 24 HR nifedipine 60 MG Extended Release Oral Tablet [Nifedical]SBD8c5b2ff0-fd2b-4915-a14c-e18ab0bdf0181
1812013Osmotic 24 HR nifedipine 60 MG Extended Release Oral TabletSCD8c5b2ff0-fd2b-4915-a14c-e18ab0bdf0181
351438Nifedical 60 MG Osmotic 24 HR Extended Release Oral TabletSY8c5b2ff0-fd2b-4915-a14c-e18ab0bdf0181
1812013nifedipine 60 MG Osmotic 24 HR Extended Release Oral TabletSY8c5b2ff0-fd2b-4915-a14c-e18ab0bdf0181

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
53808-0851-15380808510130 in 1 BLISTER PACKHistorical