Search by Drug Name or NDC

NDC 70518-2169-02 Phenazopyridine Hydrochloride 200 mg/1 Details

Phenazopyridine Hydrochloride 200 mg/1

Phenazopyridine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is PHENAZOPYRIDINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Phenazopyridine relieves urinary tract pain, burning, irritation, and discomfort, as well as urgent and frequent urination caused by urinary tract infections, surgery, injury, or examination procedures. However, phenazopyridine is not an antibiotic; it does not cure infections.

Related Packages: 70518-2169-02
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Phenazopyridine

Product Information

NDC	70518-2169
Product ID	70518-2169_030f92bf-a135-0ef3-e063-6294a90ab464
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Phenazopyridine Hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Phenazopyridine Hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	200
Active Ingredient Units	mg/1
Substance Name	PHENAZOPYRIDINE HYDROCHLORIDE
Labeler Name	REMEDYREPACK INC.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	UNAPPROVED DRUG OTHER
Application Number	n/a
Listing Certified Through	2024-12-31

Package

NDC 70518-2169-02 (70518216902)

Pricing Information	N/A
NDC Package Code	70518-2169-2
Billing NDC	70518216902
Package	21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2169-2)
Marketing Start Date	2022-05-12
NDC Exclude Flag	N