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Vasopressin
Vasopressin - 63323-302-01 - (VASOPRESSIN)
Drug Information of Vasopressin
| Product NDC: | 63323-302 |
| Proprietary Name: | Vasopressin |
| Non Proprietary Name: | VASOPRESSIN |
| Active Ingredient(s): | 20 [USP'U]/mL & nbsp; VASOPRESSIN |
| Administration Route(s): | INTRAMUSCULAR; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vasopressin
| Product NDC: | 63323-302 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20010717 |
Package Information of Vasopressin
| Package NDC: | 63323-302-01 |
| Package Description: | 25 VIAL in 1 TRAY (63323-302-01) > 1 mL in 1 VIAL |
NDC Information of Vasopressin
| NDC Code | 63323-302-01 |
| Proprietary Name | Vasopressin |
| Package Description | 25 VIAL in 1 TRAY (63323-302-01) > 1 mL in 1 VIAL |
| Product NDC | 63323-302 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | VASOPRESSIN |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; SUBCUTANEOUS |
| Start Marketing Date | 20010717 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | VASOPRESSIN |
| Strength Number | 20 |
| Strength Unit | [USP'U]/mL |
| Pharmaceutical Classes |
