Hemabate - 0009-0856-08 - (carboprost tromethamine)

Alphabetical Index


Drug Information of Hemabate

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)

Labeler Information of Hemabate

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 Information of Hemabate

Package NDC: 0009-0856-08
Package Description: 10 AMPULE in 1 PACKAGE (0009-0856-08) > 1 mL in 1 AMPULE (0009-0856-05)

NDC Information of Hemabate

NDC Code 0009-0856-08
Proprietary Name Hemabate
Package Description 10 AMPULE in 1 PACKAGE (0009-0856-08) > 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]

Complete Information of Hemabate


General Information