NDC 71335-0342

Ranitidine

Ranitidine

Ranitidine is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Ranitidine Hydrochloride.

Product ID71335-0342_961ac613-8c19-4091-ad37-a71c23a5f8a6
NDC71335-0342
Product TypeHuman Prescription Drug
Proprietary NameRanitidine
Generic NameRanitidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2008-11-19
Marketing CategoryANDA / ANDA
Application NumberANDA078542
Labeler NameBryant Ranch Prepack
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength300 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 71335-0342-1

30 TABLET, FILM COATED in 1 BOTTLE (71335-0342-1)
Marketing Start Date2009-04-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0342-3 [71335034203]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078542
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-04-22

NDC 71335-0342-4 [71335034204]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078542
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-04-22

NDC 71335-0342-5 [71335034205]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078542
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-04-22

NDC 71335-0342-9 [71335034209]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078542
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-04-22

NDC 71335-0342-2 [71335034202]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078542
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-04-22

NDC 71335-0342-7 [71335034207]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078542
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-04-22

NDC 71335-0342-8 [71335034208]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078542
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-04-22

NDC 71335-0342-1 [71335034201]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078542
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-04-22

NDC 71335-0342-6 [71335034206]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078542
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-04-22

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE300 mg/1

OpenFDA Data

SPL SET ID:8cc1dcf4-f4bb-4c9e-9e21-2db0f870ed4d
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
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.