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Sodium Chromate 51
Sodium Chromate 51 - 51808-101-02 - (Sodium Chromate 51)
Drug Information of Sodium Chromate 51
| Product NDC: | 51808-101 |
| Proprietary Name: | Sodium Chromate 51 |
| Non Proprietary Name: | Sodium Chromate 51 |
| Active Ingredient(s): | 1 mCi/5mL & nbsp; Sodium Chromate 51 |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Chromate 51
| Product NDC: | 51808-101 |
| Labeler Name: | AnazaoHealth Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120619 |
Package Information of Sodium Chromate 51
| Package NDC: | 51808-101-02 |
| Package Description: | 5 mL in 1 VIAL (51808-101-02) |
NDC Information of Sodium Chromate 51
| NDC Code | 51808-101-02 |
| Proprietary Name | Sodium Chromate 51 |
| Package Description | 5 mL in 1 VIAL (51808-101-02) |
| Product NDC | 51808-101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Chromate 51 |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120619 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | AnazaoHealth Corporation |
| Substance Name | CHROMIUM CR-51 |
| Strength Number | 1 |
| Strength Unit | mCi/5mL |
| Pharmaceutical Classes |
