Phenazopyridine HCl is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by H.j. Harkins Company, Inc.. The primary component is Phenazopyridine Hydrochloride.
| Product ID | 52959-122_76f29754-8711-434f-9548-837d2d608cfd |
| NDC | 52959-122 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Phenazopyridine HCl |
| Generic Name | Phenazopyridine Hcl |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-09-10 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE |
| Active Ingredient Strength | 200 mg/1 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2010-09-10 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-10 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-10 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-10 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-10 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-10 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-10 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-10 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-10 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-10 |
| Inactivation Date | 2019-11-13 |
| Ingredient | Strength |
|---|---|
| PHENAZOPYRIDINE HYDROCHLORIDE | 200 mg/1 |
| SPL SET ID: | 9bdc6081-e6a7-46f4-9028-c08f3c7c2dca |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 10544-055 | Phenazopyridine HCl | Phenazopyridine HCl |
| 10544-077 | Phenazopyridine HCl | Phenazopyridine HCl |
| 52959-122 | Phenazopyridine HCl | Phenazopyridine HCl |
| 69842-538 | Phenazopyridine HCl | Phenazopyridine HCl |