NDC 70408-141

RANITIDINE

Ranitidine

RANITIDINE is a Oral Syrup in the Human Prescription Drug category. It is labeled and distributed by Nostrum Laboratories, Inc.. The primary component is Ranitidine Hydrochloride.

Product ID70408-141_cb826710-66c8-436e-9c7f-e47ab8e41fab
NDC70408-141
Product TypeHuman Prescription Drug
Proprietary NameRANITIDINE
Generic NameRanitidine
Dosage FormSyrup
Route of AdministrationORAL
Marketing Start Date2011-10-03
Marketing CategoryANDA / ANDA
Application NumberANDA091091
Labeler NameNostrum Laboratories, Inc.
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength15 mg/mL
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 70408-141-34

473 mL in 1 BOTTLE (70408-141-34)
Marketing Start Date2011-10-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70408-141-34 [70408014134]

RANITIDINE SYRUP
Marketing CategoryANDA
Application NumberANDA091091
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2011-10-03

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE15 mg/mL

OpenFDA Data

SPL SET ID:93d1d088-1ebb-478e-9715-de067052bff3
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 705610
  • UPC Code
  • 0370408141347
  • Pharmacological Class

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

    Medicade Reported Pricing

    70408014134 RANITIDINE 15 MG/ML SYRUP

    Pricing Unit: ML | 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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.