VITAMIN K1 (PHYTONADIONE)
Summary
FDA approved VITAMIN K1 (PHYTONADIONE) by HOSPIRA. ANDA (Generic) approval (Labeling) on 2026-03-06. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
ANDA087955-33
Action Date
2026-03-06
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
VITAMIN K1 (generic: PHYTONADIONE), INJECTABLE, INJECTION. Application: ANDA087955
Company
Context & Analysis
HOSPIRA has 52 FDA actions in our database.
Frequently Asked Questions
How often does HOSPIRA have FDA actions?
HOSPIRA has 52 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA087955-33" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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