Product NDC: | 54365-200 |
Proprietary Name: | Blood Culture Prep Kit |
Non Proprietary Name: | Isopropyl alcohol and iodine |
Active Ingredient(s): | & nbsp; Isopropyl alcohol and iodine |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54365-200 |
Labeler Name: | CareFusion 213 LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19880201 |
Package NDC: | 54365-200-99 |
Package Description: | 1 KIT in 1 POUCH (54365-200-99) * 1.1 mL in 1 APPLICATOR (54365-170-02) * .67 mL in 1 AMPULE (54365-161-01) |
NDC Code | 54365-200-99 |
Proprietary Name | Blood Culture Prep Kit |
Package Description | 1 KIT in 1 POUCH (54365-200-99) * 1.1 mL in 1 APPLICATOR (54365-170-02) * .67 mL in 1 AMPULE (54365-161-01) |
Product NDC | 54365-200 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Isopropyl alcohol and iodine |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 19880201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | CareFusion 213 LLC |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |