NDC 64679-741

RANITIDINE

Ranitidine

RANITIDINE is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Wockhardt Usa Llc.. The primary component is Ranitidine Hydrochloride.

Product ID64679-741_b389e8a7-8065-48f9-a0bc-fb30bed04c2d
NDC64679-741
Product TypeHuman Otc Drug
Proprietary NameRANITIDINE
Generic NameRanitidine
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2007-11-26
Marketing CategoryANDA / ANDA
Application NumberANDA078653
Labeler NameWockhardt USA LLC.
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength150 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 64679-741-00

30000 TABLET, COATED in 1 DRUM (64679-741-00)
Marketing Start Date2007-11-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 64679-741-02 [64679074102]

RANITIDINE TABLET, COATED
Marketing CategoryANDA
Application NumberANDA078653
Product TypeHUMAN OTC DRUG
Marketing Start Date2007-11-26

NDC 64679-741-05 [64679074105]

RANITIDINE TABLET, COATED
Marketing CategoryANDA
Application NumberANDA078653
Product TypeHUMAN OTC DRUG
Marketing Start Date2007-11-26

NDC 64679-741-01 [64679074101]

RANITIDINE TABLET, COATED
Marketing CategoryANDA
Application NumberANDA078653
Product TypeHUMAN OTC DRUG
Marketing Start Date2007-11-26

NDC 64679-741-00 [64679074100]

RANITIDINE TABLET, COATED
Marketing CategoryANDA
Application NumberANDA078653
Product TypeHUMAN OTC DRUG
Marketing Start Date2007-11-26

NDC 64679-741-03 [64679074103]

RANITIDINE TABLET, COATED
Marketing CategoryANDA
Application NumberANDA078653
Product TypeHUMAN OTC DRUG
Marketing Start Date2007-11-26

NDC 64679-741-06 [64679074106]

RANITIDINE TABLET, COATED
Marketing CategoryANDA
Application NumberANDA078653
Product TypeHUMAN OTC DRUG
Marketing Start Date2007-11-26

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:f7aa08fc-5d10-4067-8f20-3c3e176e3e35
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198191

    • 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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