AZO is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by I-health, Inc.. The primary component is Phenazopyridine Hydrochloride.
| Product ID | 49973-245_56beb1e5-88e1-43b7-b402-c7ab501a0d78 |
| NDC | 49973-245 |
| Product Type | Human Otc Drug |
| Proprietary Name | AZO |
| Generic Name | Urinary Pain Relief |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2014-03-04 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | i-Health, Inc. |
| Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE |
| Active Ingredient Strength | 98 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2014-03-04 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-03-04 |
| Marketing End Date | 2017-02-01 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-03-04 |
| Marketing End Date | 2017-02-01 |
| Ingredient | Strength |
|---|---|
| PHENAZOPYRIDINE HYDROCHLORIDE | 97.5 mg/1 |
| SPL SET ID: | 2cf863e1-cd38-47a9-8c52-3dac465e9034 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 49973-244 | AZO | Urinary Pain Relief |
| 49973-245 | AZO | Urinary Pain Relief |
| 49973-301 | AZO | Urinary Pain Relief |
| 49973-606 | AZO | Eupatorium Perfoliatum Flowering Top and Viscum Album Leaf |
| 49973-667 | AZO | Candida Albicans, Wood Creosote, Sodium Chloride, and Sulfur |