Product NDC: | 0009-0856 |
Proprietary Name: | Hemabate |
Non Proprietary Name: | carboprost tromethamine |
Active Ingredient(s): | 250 ug/mL & nbsp; carboprost tromethamine |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0009-0856 |
Labeler Name: | Pharmacia and Upjohn Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017989 |
Marketing Category: | NDA |
Start Marketing Date: | 19790109 |
Package NDC: | 0009-0856-05 |
Package Description: | 1 mL in 1 AMPULE (0009-0856-05) |
NDC Code | 0009-0856-05 |
Proprietary Name | Hemabate |
Package Description | 1 mL in 1 AMPULE (0009-0856-05) |
Product NDC | 0009-0856 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | carboprost tromethamine |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 19790109 |
Marketing Category Name | NDA |
Labeler Name | Pharmacia and Upjohn Company |
Substance Name | CARBOPROST TROMETHAMINE |
Strength Number | 250 |
Strength Unit | ug/mL |
Pharmaceutical Classes | Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] |