| 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] |