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NITHIODOTE
NITHIODOTE - 60267-812-00 - (Sodium Nitrite and Sodium Thiosulfate)
Drug Information of NITHIODOTE
| Product NDC: | 60267-812 |
| Proprietary Name: | NITHIODOTE |
| Non Proprietary Name: | Sodium Nitrite and Sodium Thiosulfate |
| Active Ingredient(s): | & nbsp; Sodium Nitrite and Sodium Thiosulfate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NITHIODOTE
| Product NDC: | 60267-812 |
| Labeler Name: | Hope Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA201444 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110114 |
Package Information of NITHIODOTE
| Package NDC: | 60267-812-00 |
| Package Description: | 1 KIT in 1 CARTON (60267-812-00) * 10 mL in 1 VIAL, SINGLE-USE (60267-311-10) * 50 mL in 1 VIAL, SINGLE-USE (60267-705-50) |
NDC Information of NITHIODOTE
| NDC Code | 60267-812-00 |
| Proprietary Name | NITHIODOTE |
| Package Description | 1 KIT in 1 CARTON (60267-812-00) * 10 mL in 1 VIAL, SINGLE-USE (60267-311-10) * 50 mL in 1 VIAL, SINGLE-USE (60267-705-50) |
| Product NDC | 60267-812 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Nitrite and Sodium Thiosulfate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110114 |
| Marketing Category Name | NDA |
| Labeler Name | Hope Pharmaceuticals |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
