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Drug profile · INN

vitamin a palmitate

VITAMIN A PALMITATE

approved
US status
approved
Patents linked
5
News articles
0

Quick answer

vitamin a palmitate (VITAMIN A PALMITATE) is an FDA-listed pharmaceutical active ingredient. Associated with Teva Pharma GmbH. Route of administration: injection. Current US regulatory status: approved.

Key facts

INN vitamin a palmitate
Brand VITAMIN A PALMITATE
Route INJECTION
Formulation INJECTABLE
Originator Teva Pharma GmbH

Related patents

Search patents →

  1. US 12364671

    Methods of administering vitamin A and lactic acid to gilts

    Expires Mon Jul 17 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

  2. US 11484591

    Chemoprevention using controlled-release formulations of anti-interleukin 6 agents, synthetic vitamin A analogues or metabolites, and estradiol metabolites

    Expires Mon Oct 27 2042 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

  3. US 8063250

    Crystal forms of O-desmethylvenlafaxine fumarate

    Expires Mon Nov 17 2031 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

  4. US 7674935

    Crystal forms of O-desmethylvenlafaxine

    Expires Mon Mar 04 2030 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

  5. US 7605290

    Processes for the synthesis of O-desmethylvenlafaxine

    Expires Mon Oct 15 2029 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

Frequently asked questions

What is vitamin a palmitate?

vitamin a palmitate (VITAMIN A PALMITATE) is an FDA-listed pharmaceutical active ingredient. Associated with Teva Pharma GmbH. Route of administration: injection. Current US regulatory status: approved.

What is the brand name for vitamin a palmitate?

VITAMIN A PALMITATE is a marketed brand name for vitamin a palmitate. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of vitamin a palmitate?

vitamin a palmitate has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.