NDC 55648-447

RANITIDINE

Ranitidine Hydrochloride

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

Product ID55648-447_fda4671d-cce2-44b4-b41c-caa6ca7ecbec
NDC55648-447
Product TypeHuman Prescription Drug
Proprietary NameRANITIDINE
Generic NameRanitidine Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-12-11
Marketing CategoryANDA / ANDA
Application NumberANDA078701
Labeler NameWOCKHARDT LIMITED
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 55648-447-02

100 TABLET in 1 BOTTLE (55648-447-02)
Marketing Start Date2009-12-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55648-447-07 [55648044707]

RANITIDINE TABLET
Marketing CategoryANDA
Application NumberANDA078701
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-01-02
Inactivation Date2020-01-31

NDC 55648-447-03 [55648044703]

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

NDC 55648-447-05 [55648044705]

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

NDC 55648-447-02 [55648044702]

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

NDC 55648-447-04 [55648044704]

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

NDC 55648-447-06 [55648044706]

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

NDC 55648-447-01 [55648044701]

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:c79c92e0-1e7b-4854-a99a-1a22eed3c333
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198193
  • 198191
    • UPC Code
  • 0364679447062
  • 0364679742044
  • 0364679447048

    • Pharmacological Class

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

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

    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
    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
    10544-438RanitidineRanitidine
    10544-056RanitidineRanitidine
    10544-516RanitidineRanitidine
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