NDC 21695-109

Ranitidine

Ranitidine

Ranitidine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Rebel Distributors. The primary component is Ranitidine Hydrochloride.

Product ID21695-109_dcee67ac-e58c-4050-ad16-f8253a17036b
NDC21695-109
Product TypeHuman Prescription Drug
Proprietary NameRanitidine
Generic NameRanitidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-12-17
Marketing CategoryANDA / ANDA
Application NumberANDA077824
Labeler NameRebel Distributors
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength150 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 21695-109-90

90 TABLET in 1 BOTTLE (21695-109-90)
Marketing Start Date2009-12-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 21695-109-60 [21695010960]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-17
Inactivation Date2019-09-24

NDC 21695-109-90 [21695010990]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-17
Inactivation Date2019-09-24

NDC 21695-109-72 [21695010972]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-17
Inactivation Date2019-09-24

NDC 21695-109-14 [21695010914]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-17
Inactivation Date2019-09-24

NDC 21695-109-00 [21695010900]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-17
Inactivation Date2019-09-24

NDC 21695-109-30 [21695010930]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-17
Inactivation Date2019-09-24

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:a9fef8f6-b823-4b8a-84b8-2b916374adb5
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198193
  • 198191

    • Pharmacological Class

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

    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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