Last Updated: May 10, 2026

Details for New Drug Application (NDA): 017989

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NDA 017989 describes HEMABATE, which is a drug marketed by Pfizer and is included in one NDA. It is available from one supplier. Additional details are available on the HEMABATE profile page.

The generic ingredient in HEMABATE is carboprost tromethamine. There is one drug master file entry for this compound. Twenty-one suppliers are listed for this compound. Additional details are available on the carboprost tromethamine profile page.

Summary for 017989

Tradename:	HEMABATE
Applicant:	Pfizer
Ingredient:	carboprost tromethamine
Patents:	0

Pharmacology for NDA: 017989

Medical Subject Heading (MeSH) Categories for 017989

Abortifacient Agents, Nonsteroidal
Oxytocics

Suppliers and Packaging for NDA: 017989

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
HEMABATE	carboprost tromethamine	INJECTABLE;INJECTION	017989	NDA	Pharmacia & Upjohn Company LLC	0009-0856	0009-0856-05	1 mL in 1 AMPULE (0009-0856-05)
HEMABATE	carboprost tromethamine	INJECTABLE;INJECTION	017989	NDA	Pharmacia & Upjohn Company LLC	0009-0856	0009-0856-08	10 AMPULE in 1 PACKAGE (0009-0856-08) / 1 mL in 1 AMPULE (0009-0856-05)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	INJECTABLE;INJECTION			Strength	EQ 0.25MG BASE/ML
Approval Date:	Approved Prior to Jan 1, 1982	TE:	AP	RLD:	Yes

Expired US Patents for NDA 017989

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Pfizer	HEMABATE	carboprost tromethamine	INJECTABLE;INJECTION	017989-001	Approved Prior to Jan 1, 1982	3,728,382	⤷ Start Trial
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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