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I 131 Mini
I 131 Mini - 51808-119-01 - (I 131 Mini)
Drug Information of I 131 Mini
| Product NDC: | 51808-119 |
| Proprietary Name: | I 131 Mini |
| Non Proprietary Name: | I 131 Mini |
| Active Ingredient(s): | 500 mCi/1 & nbsp; I 131 Mini |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of I 131 Mini
| Product NDC: | 51808-119 |
| Labeler Name: | AnazaoHealth Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120523 |
Package Information of I 131 Mini
| Package NDC: | 51808-119-01 |
| Package Description: | 3 CAPSULE in 1 VIAL (51808-119-01) |
NDC Information of I 131 Mini
| NDC Code | 51808-119-01 |
| Proprietary Name | I 131 Mini |
| Package Description | 3 CAPSULE in 1 VIAL (51808-119-01) |
| Product NDC | 51808-119 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | I 131 Mini |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120523 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | AnazaoHealth Corporation |
| Substance Name | SODIUM IODIDE I-131 |
| Strength Number | 500 |
| Strength Unit | mCi/1 |
| Pharmaceutical Classes |
