NDC 64679-906

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 ID64679-906_44a635c5-5c3a-41a5-b882-43fca6d43526
NDC64679-906
Product TypeHuman Prescription Drug
Proprietary NameRANITIDINE
Generic NameRanitidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1998-12-17
Marketing CategoryANDA / ANDA
Application NumberANDA075208
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 64679-906-01

60 TABLET in 1 BOTTLE (64679-906-01)
Marketing Start Date1998-12-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 64679-906-01 [64679090601]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA075208
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-12-17

NDC 64679-906-06 [64679090606]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA075208
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-12-17

NDC 64679-906-12 [64679090612]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA075208
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-12-17

NDC 64679-906-03 [64679090603]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA075208
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-12-17

NDC 64679-906-02 [64679090602]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA075208
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-12-17

NDC 64679-906-05 [64679090605]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA075208
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-12-17

NDC 64679-906-04 [64679090604]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA075208
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1998-12-17

NDC 64679-906-11 [64679090611]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA075208
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-12-17

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:da16ec36-5824-48e0-856a-16518e588675
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198193
  • 198191

    • Pharmacological Class

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

    Medicade Reported Pricing

    64679090606 RANITIDINE 150 MG TABLET

    Pricing Unit: EA | Drug Type:

    64679090603 RANITIDINE 150 MG TABLET

    Pricing Unit: EA | Drug Type:

    64679090601 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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