NDC 0069-2650

Procardia XL

Nifedipine

Procardia XL is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Pfizer Laboratories Div Pfizer Inc. The primary component is Nifedipine.

Product ID0069-2650_0a3e20ea-15e2-4b03-b400-8e2d46804d13
NDC0069-2650
Product TypeHuman Prescription Drug
Proprietary NameProcardia XL
Generic NameNifedipine
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date1989-09-06
Marketing CategoryNDA / NDA
Application NumberNDA019684
Labeler NamePfizer Laboratories Div Pfizer Inc
Substance NameNIFEDIPINE
Active Ingredient Strength30 mg/1
Pharm ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0069-2650-41

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0069-2650-41)
Marketing Start Date1989-09-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0069-2650-94 [00069265094]

Procardia XL TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019684
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1989-09-06
Marketing End Date2011-04-11

NDC 0069-2650-41 [00069265041]

Procardia XL TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019684
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1989-09-06

NDC 0069-2650-72 [00069265072]

Procardia XL TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019684
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1989-09-06

NDC 0069-2650-66 [00069265066]

Procardia XL TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019684
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1989-09-06

Drug Details

Active Ingredients

IngredientStrength
NIFEDIPINE30 mg/1

OpenFDA Data

SPL SET ID:8ebcb33c-f43b-4b36-9f94-9774b2a59e06
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 207773
  • 207772
  • 1812015
  • 1812013
  • 1812011
  • 207774

    • Pharmacological Class

    • Calcium Channel Antagonists [MoA]
    • Dihydropyridine Calcium Channel Blocker [EPC]
    • Dihydropyridines [CS]

    NDC Crossover Matching brand name "Procardia XL" or generic name "Nifedipine"

    NDCBrand NameGeneric Name
    70518-0600Procardia XLProcardia XL
    0228-2497NifedipineNifedipine
    0228-2530NifedipineNifedipine
    0378-0353Nifedipinenifedipine
    0378-0360Nifedipinenifedipine
    0378-0390Nifedipinenifedipine
    0378-0480Nifedipinenifedipine
    0378-0481Nifedipinenifedipine
    0378-0494Nifedipinenifedipine
    0615-5541Nifedipinenifedipine
    0615-6563Nifedipinenifedipine
    0615-7571NifedipineNifedipine
    0904-6544NifedipineNifedipine
    0904-6545NifedipineNifedipine
    0904-7080Nifedipinenifedipine
    0904-7081Nifedipinenifedipine
    0904-7082Nifedipinenifedipine
    0904-7208NifedipineNifedipine
    0904-7229NifedipineNifedipine
    10370-677NifedipineNifedipine
    10370-678NifedipineNifedipine
    10370-679NifedipineNifedipine
    21695-807nifedipinenifedipine
    21695-908nifedipinenifedipine
    21695-909NifedipineNifedipine
    23155-194NifedipineNifedipine
    23155-195NifedipineNifedipine
    0069-2600Procardianifedipine
    0069-2650Procardianifedipine
    0069-2660Procardianifedipine
    0069-2670Procardianifedipine

    Trademark Results [Procardia]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    PROCARDIA
    PROCARDIA
    73207504 1135469 Live/Registered
    PFIZER INC.
    1979-03-15
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.