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AZO
AZO - 49973-244-12 - (Urinary Pain Relief)
Drug Information of AZO
| Product NDC: | 49973-244 |
| Proprietary Name: | AZO |
| Non Proprietary Name: | Urinary Pain Relief |
| Active Ingredient(s): | 97.5 mg/1 & nbsp; Urinary Pain Relief |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AZO
| Product NDC: | 49973-244 |
| Labeler Name: | i-Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120518 |
Package Information of AZO
| Package NDC: | 49973-244-12 |
| Package Description: | 6 BLISTER PACK in 1 BOX (49973-244-12) > 2 TABLET in 1 BLISTER PACK |
NDC Information of AZO
| NDC Code | 49973-244-12 |
| Proprietary Name | AZO |
| Package Description | 6 BLISTER PACK in 1 BOX (49973-244-12) > 2 TABLET in 1 BLISTER PACK |
| Product NDC | 49973-244 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Urinary Pain Relief |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120518 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | i-Health, Inc. |
| Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE |
| Strength Number | 97.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
