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NDC 70954-0496-10 Nitrofurantoin 25 mg/5mL Details

Nitrofurantoin 25 mg/5mL

Nitrofurantoin is a ORAL SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by ANI Pharmaceuticals, Inc.. The primary component is NITROFURANTOIN.

MedlinePlus Drug Summary

Nitrofurantoin is used to treat urinary tract infections. Nitrofurantoin is in a class of medications called antibiotics. It works by killing bacteria that cause infection. Antibiotics such as nitrofurantoin will not work for colds, flu, or other viral infections. Using antibiotics when they are not needed increases your risk of getting an infection later that resists antibiotic treatment.

Related Packages: 70954-0496-10
Last Updated: 05/12/2024
MedLinePlus Full Drug Details: Nitrofurantoin

Product Information

NDC	70954-0496
Product ID	70954-496_3b377aff-2d4b-43ea-84c9-8e72c1421b7b
Associated GPIs
GCN Sequence Number	009434
GCN Sequence Number Description	nitrofurantoin ORAL SUSP 25 MG/5 ML ORAL
HIC3	W2F
HIC3 Description	NITROFURAN DERIVATIVES ANTIBACTERIAL AGENTS
GCN	41870
HICL Sequence Number	004089
HICL Sequence Number Description	NITROFURANTOIN
Brand/Generic	Generic
Proprietary Name	Nitrofurantoin
Proprietary Name Suffix	n/a
Non-Proprietary Name	Nitrofurantoin
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	SUSPENSION
Route	ORAL
Active Ingredient Strength	25
Active Ingredient Units	mg/5mL
Substance Name	NITROFURANTOIN
Labeler Name	ANI Pharmaceuticals, Inc.
Pharmaceutical Class	Nitrofuran Antibacterial [EPC], Nitrofurans [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA216385
Listing Certified Through	2024-12-31

Package

NDC 70954-0496-10 (70954049610)

Pricing Information	N/A
NDC Package Code	70954-496-10
Billing NDC	70954049610
Package	230 mL in 1 BOTTLE (70954-496-10)
Marketing Start Date	2023-04-17
NDC Exclude Flag	N