NDC 68151-2103

Rimantadine Hydrochloride

Rimantadine Hydrochloride

Rimantadine Hydrochloride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Carilion Materials Management. The primary component is Rimantadine Hydrochloride.

Product ID68151-2103_fc97c5f7-872a-4268-afdb-001dd07762c9
NDC68151-2103
Product TypeHuman Prescription Drug
Proprietary NameRimantadine Hydrochloride
Generic NameRimantadine Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2005-04-01
Marketing CategoryANDA / ANDA
Application NumberANDA076132
Labeler NameCarilion Materials Management
Substance NameRIMANTADINE HYDROCHLORIDE
Active Ingredient Strength100 mg/1
Pharm ClassesInfluenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 68151-2103-0

1 TABLET, FILM COATED in 1 PACKAGE (68151-2103-0)
Marketing Start Date2005-04-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68151-2103-0 [68151210300]

Rimantadine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076132
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-04-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
RIMANTADINE HYDROCHLORIDE100 mg/1

OpenFDA Data

SPL SET ID:a1d00c0f-ec9d-4849-b3b5-9c0dff07026c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 856605
  • Pharmacological Class

    • Influenza A M2 Protein Inhibitor [EPC]
    • M2 Protein Inhibitors [MoA]

    NDC Crossover Matching brand name "Rimantadine Hydrochloride" or generic name "Rimantadine Hydrochloride"

    NDCBrand NameGeneric Name
    0115-1911Rimantadine HydrochlorideRimantadine Hydrochloride
    52959-305Rimantadine HydrochlorideRimantadine Hydrochloride
    63629-3552Rimantadine HydrochlorideRimantadine Hydrochloride
    68151-2103Rimantadine HydrochlorideRimantadine Hydrochloride

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