NDC 65841-260

Ribavirin

Ribavirin

Ribavirin is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Cadila Healthcare Limited. The primary component is Ribavirin.

Product ID65841-260_061eb9f8-611d-449e-97f3-ccc9614ca18e
NDC65841-260
Product TypeHuman Prescription Drug
Proprietary NameRibavirin
Generic NameRibavirin
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2006-01-25
Marketing CategoryANDA / ANDA
Application NumberANDA077224
Labeler NameCadila Healthcare Limited
Substance NameRIBAVIRIN
Active Ingredient Strength200 mg/1
Pharm ClassesNucleoside Analog [EXT],Nucleoside Analog Antiviral [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 65841-260-03

168 CAPSULE in 1 BOTTLE (65841-260-03)
Marketing Start Date2006-01-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65841-260-30 [65841026030]

Ribavirin CAPSULE
Marketing CategoryANDA
Application NumberANDA077224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-25

NDC 65841-260-13 [65841026013]

Ribavirin CAPSULE
Marketing CategoryANDA
Application NumberANDA077224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-25

NDC 65841-260-09 [65841026009]

Ribavirin CAPSULE
Marketing CategoryANDA
Application NumberANDA077224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-25

NDC 65841-260-28 [65841026028]

Ribavirin CAPSULE
Marketing CategoryANDA
Application NumberANDA077224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-25

NDC 65841-260-07 [65841026007]

Ribavirin CAPSULE
Marketing CategoryANDA
Application NumberANDA077224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-25

NDC 65841-260-03 [65841026003]

Ribavirin CAPSULE
Marketing CategoryANDA
Application NumberANDA077224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-25

NDC 65841-260-10 [65841026010]

Ribavirin CAPSULE
Marketing CategoryANDA
Application NumberANDA077224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-25

NDC 65841-260-04 [65841026004]

Ribavirin CAPSULE
Marketing CategoryANDA
Application NumberANDA077224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-25

NDC 65841-260-12 [65841026012]

Ribavirin CAPSULE
Marketing CategoryANDA
Application NumberANDA077224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-25

Drug Details

Active Ingredients

IngredientStrength
RIBAVIRIN200 mg/1

OpenFDA Data

SPL SET ID:b97cd49c-9e19-4a35-987c-06e62bb25b6b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 312817
  • Pharmacological Class

    • Nucleoside Analog [EXT]
    • Nucleoside Analog Antiviral [EPC]

    NDC Crossover Matching brand name "Ribavirin" or generic name "Ribavirin"

    NDCBrand NameGeneric Name
    0781-2043RibavirinRibavirin
    0781-5177RibavirinRibavirin
    42494-423RibavirinRibavirin
    53808-0781RibavirinRIBAVIRIN
    53808-0782RibavirinRIBAVIRIN
    54738-950ribavirinribavirin
    54738-951ribavirinribavirin
    54738-952ribavirinribavirin
    54738-953ribavirinribavirin
    63629-2149RibavirinRibavirin
    65841-046RibavirinRibavirin
    65841-129RibavirinRibavirin
    65841-260RibavirinRibavirin
    65841-603RibavirinRibavirin
    65841-632RibavirinRibavirin
    65862-207RibavirinRibavirin
    68084-179RibavirinRibavirin
    68382-046RibavirinRibavirin
    68382-260RibavirinRibavirin
    68382-129RibavirinRibavirin
    68382-128RibavirinRibavirin
    68382-395RIBAVIRINRIBAVIRIN
    68382-127RibavirinRibavirin
    68682-019RibavirinRibavirin
    65862-290RibavirinRibavirin
    68475-003RIBAVIRINRIBAVIRIN
    0074-3197ModeribaRibavirin
    0074-3282ModeribaRibavirin
    0085-1318REBETOLribavirin
    0187-0007VirazoleRibavirin

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