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NDC 71335-1805-06 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: 71335-1805-06Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Phenazopyridine
Product Information
| NDC | 71335-1805 |
|---|---|
| Product ID | 71335-1805_ebdf1127-3e12-44ae-a3e2-a30cde4efcb1 |
| Associated GPIs | 56300010100310 |
| GCN Sequence Number | 009478 |
| GCN Sequence Number Description | phenazopyridine HCl TABLET 200 MG ORAL |
| HIC3 | R5A |
| HIC3 Description | URINARY TRACT ANESTHETIC/ANALGESIC AGNT (AZO-DYE) |
| GCN | 42122 |
| HICL Sequence Number | 004108 |
| HICL Sequence Number Description | PHENAZOPYRIDINE HCL |
| Brand/Generic | Generic |
| 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 | 2024-12-31 |
Package
NDC 71335-1805-06 (71335180506)
| NDC Package Code | 71335-1805-6 |
|---|---|
| Billing NDC | 71335180506 |
| Package | 6 TABLET in 1 BOTTLE (71335-1805-6) |
| Marketing Start Date | 2021-04-07 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |