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AZO
AZO - 49973-606-60 - (Eupatorium Perfoliatum Flowering Top and Viscum Album Leaf)
Drug Information of AZO
| Product NDC: | 49973-606 |
| Proprietary Name: | AZO |
| Non Proprietary Name: | Eupatorium Perfoliatum Flowering Top and Viscum Album Leaf |
| Active Ingredient(s): | 5; 5 [hp_X]/1; [hp_X]/1 & nbsp; Eupatorium Perfoliatum Flowering Top and Viscum Album Leaf |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AZO
| Product NDC: | 49973-606 |
| Labeler Name: | i-Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120522 |
Package Information of AZO
| Package NDC: | 49973-606-60 |
| Package Description: | 60 BLISTER PACK in 1 BOX (49973-606-60) > 1 TABLET in 1 BLISTER PACK |
NDC Information of AZO
| NDC Code | 49973-606-60 |
| Proprietary Name | AZO |
| Package Description | 60 BLISTER PACK in 1 BOX (49973-606-60) > 1 TABLET in 1 BLISTER PACK |
| Product NDC | 49973-606 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Eupatorium Perfoliatum Flowering Top and Viscum Album Leaf |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120522 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | i-Health, Inc. |
| Substance Name | EUPATORIUM PERFOLIATUM FLOWERING TOP; VISCUM ALBUM LEAF |
| Strength Number | 5; 5 |
| Strength Unit | [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes |
