NDC 62037-599

Cartia XT

Diltiazem Hydrochloride

Cartia XT is a Oral Capsule, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Actavis Pharma, Inc.. The primary component is Diltiazem Hydrochloride.

Product ID62037-599_3f024ff2-56ff-480e-b639-c9b794318fbe
NDC62037-599
Product TypeHuman Prescription Drug
Proprietary NameCartia XT
Generic NameDiltiazem Hydrochloride
Dosage FormCapsule, Extended Release
Route of AdministrationORAL
Marketing Start Date1998-07-09
Marketing CategoryANDA / ANDA
Application NumberANDA074752
Labeler NameActavis Pharma, Inc.
Substance NameDILTIAZEM HYDROCHLORIDE
Active Ingredient Strength240 mg/1
Pharm ClassesCalcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 62037-599-05

500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-599-05)
Marketing Start Date1999-06-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62037-599-90 [62037059990]

Cartia XT CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074752
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1999-06-23

NDC 62037-599-07 [62037059907]

Cartia XT CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074752
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-07-09
Marketing End Date1998-07-09

NDC 62037-599-05 [62037059905]

Cartia XT CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074752
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1999-06-23

NDC 62037-599-10 [62037059910]

Cartia XT CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074752
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-07-09
Marketing End Date1998-07-09

NDC 62037-599-30 [62037059930]

Cartia XT CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA074752
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-07-09
Marketing End Date1998-07-09

Drug Details

Active Ingredients

IngredientStrength
DILTIAZEM HYDROCHLORIDE240 mg/1

OpenFDA Data

SPL SET ID:2dc2b889-8443-4f7f-83be-86c68e179804
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 831338
  • 830861
  • 831309
  • 831226
  • 830801
  • 830837
  • 831255
  • 830845

    • Pharmacological Class

    • Calcium Channel Antagonists [MoA]
    • Calcium Channel Blocker [EPC]

    Medicade Reported Pricing

    62037059990 CARTIA XT 240 MG CAPSULE

    Pricing Unit: EA | Drug Type:

    62037059905 CARTIA XT 240 MG CAPSULE

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Cartia XT" or generic name "Diltiazem Hydrochloride"

    NDCBrand NameGeneric Name
    70518-1537Cartia XTCartia XT
    71335-0879Cartia XTCartia XT
    50090-3124Cartia XTCartia XT
    50090-3051Cartia XTCartia XT
    62037-597Cartia XTCartia XT
    62037-600Cartia XTCartia XT
    62037-599Cartia XTCartia XT
    62037-598Cartia XTCartia XT
    63629-7896Cartia XTCartia XT
    0187-0771CardizemDiltiazem Hydrochloride
    0187-0772CardizemDiltiazem Hydrochloride
    0187-0792CardizemDiltiazem Hydrochloride
    0187-0795Cardizem CDdiltiazem hydrochloride
    0187-0796Cardizem CDdiltiazem hydrochloride
    0187-0797Cardizem CDdiltiazem hydrochloride
    0093-0318Diltiazem HydrochlorideDiltiazem Hydrochloride
    0093-0319Diltiazem HydrochlorideDiltiazem Hydrochloride
    0093-0320Diltiazem HydrochlorideDiltiazem Hydrochloride
    0093-0321Diltiazem HydrochlorideDiltiazem Hydrochloride

    Trademark Results [Cartia]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    CARTIA
    CARTIA
    75979634 2392379 Dead/Cancelled
    CARTIA, INC.
    1998-05-26
    CARTIA
    CARTIA
    75491241 not registered Dead/Abandoned
    CARTIA, INC.
    1998-05-26
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