NDC 64679-447

RANITIDINE

Ranitidine

RANITIDINE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Wockhardt Usa Llc.. The primary component is Ranitidine Hydrochloride.

Product ID64679-447_c63eb133-3d21-4f57-a3a4-07e8f59fe6a1
NDC64679-447
Product TypeHuman Prescription Drug
Proprietary NameRANITIDINE
Generic NameRanitidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-12-11
Marketing CategoryANDA / ANDA
Application NumberANDA078701
Labeler NameWockhardt USA LLC.
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength150 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 64679-447-07

6000 TABLET in 1 DRUM (64679-447-07)
Marketing Start Date2009-12-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 64679-447-04 [64679044704]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA078701
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

NDC 64679-447-07 [64679044707]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA078701
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

NDC 64679-447-01 [64679044701]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA078701
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

NDC 64679-447-02 [64679044702]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA078701
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

NDC 64679-447-05 [64679044705]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA078701
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

NDC 64679-447-06 [64679044706]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA078701
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

NDC 64679-447-03 [64679044703]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA078701
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-11
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:befbaee8-0e3e-45e4-afd2-9afbae048455
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198193
  • 198191
    • UPC Code
  • 0364679742044
  • 0364679447048

    • Pharmacological Class

    • Histamine H2 Receptor Antagonists [MoA]
    • Histamine-2 Receptor Antagonist [EPC]

    Medicade Reported Pricing

    64679044706 RANITIDINE 150 MG TABLET

    Pricing Unit: EA | Drug Type:

    64679044704 RANITIDINE 150 MG TABLET

    Pricing Unit: EA | Drug Type:

    64679044702 RANITIDINE 150 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "RANITIDINE" or generic name "Ranitidine"

    NDCBrand NameGeneric Name
    0121-0727RanitidineRANITIDINE
    0121-4727RanitidineRANITIDINE
    0172-4357RanitidineRanitidine
    0172-4358RanitidineRanitidine
    0363-0352RanitidineRanitidine
    0440-2300RanitidineRanitidine Hydrochloride
    0440-8300RanitidineRanitidine
    0440-8305RanitidineRanitidine
    0615-4513RanitidineRanitidine
    0615-4514RanitidineRanitidine
    0615-8021RanitidineRanitidine
    0781-6087RanitidineRanitidine
    0904-6349RanitidineRanitidine
    0904-6716RanitidineRanitidine
    0904-6921RanitidineRanitidine
    10544-056RanitidineRanitidine
    10544-438RanitidineRanitidine
    10544-516RanitidineRanitidine
    68071-2190RanitidineRanitidine
    68071-3162RanitidineRanitidine
    68071-3317RanitidineRanitidine
    68071-2185RanitidineRanitidine
    68071-3248RanitidineRanitidine
    68071-3165RanitidineRanitidine
    68151-1610RanitidineRanitidine
    68151-2890RanitidineRanitidine
    68462-248RanitidineRanitidine
    68462-249RanitidineRanitidine
    68788-6382RanitidineRanitidine
    68788-7101RanitidineRanitidine
    68788-7078RanitidineRanitidine
    68788-7388RanitidineRanitidine
    68788-9875RanitidineRanitidine
    68788-9874RanitidineRanitidine
    70408-141RANITIDINERANITIDINE
    70518-0222RanitidineRanitidine
    70518-0263RanitidineRanitidine
    70518-0093RanitidineRanitidine
    70518-0622RanitidineRanitidine
    70518-0873RanitidineRanitidine
    70518-0801RanitidineRanitidine
    70518-1361RanitidineRanitidine
    70518-1714RanitidineRanitidine
    70934-017RanitidineRanitidine
    71141-013RanitidineRanitidine
    71335-0394RanitidineRanitidine
    71335-0342RanitidineRanitidine
    71335-0363RanitidineRanitidine
    71821-001RanitidineRanitidine
    71821-002RanitidineRanitidine
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