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NDC 71335-1399-09 Phenazopyridine Hydrochloride 200 mg/1 Details

Phenazopyridine Hydrochloride 200 mg/1

Phenazopyridine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. 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: 71335-1399-09
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Phenazopyridine

Product Information

NDC	71335-1399
Product ID	71335-1399_9258afaa-84df-4975-b140-5d3731f80139
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
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	200
Active Ingredient Units	mg/1
Substance Name	PHENAZOPYRIDINE HYDROCHLORIDE
Labeler Name	Bryant Ranch Prepack
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	UNAPPROVED DRUG OTHER
Application Number	n/a
Listing Certified Through	2022-12-31

Package

NDC 71335-1399-09 (71335139909)

Pricing Information	N/A
NDC Package Code	71335-1399-9
Billing NDC	71335139909
Package	18 TABLET in 1 BOTTLE (71335-1399-9)
Marketing Start Date	2011-02-01
NDC Exclude Flag	N