MedPath

DL-alpha tocopheryl acetate

Generic Name
DL-alpha tocopheryl acetate
Brand Names
Mvi Pediatric, Natafort
Drug Type
Small Molecule
Chemical Formula
C31H52O3
CAS Number
52225-20-4
Unique Ingredient Identifier
WR1WPI7EW8

Overview

No overview information available.

Indication

No indication information available.

Associated Conditions

  • Degenerative Retinal Disorders
  • Eye degenerative disorder
  • Vitamin Deficiency
  • Vitamin E Deficiency

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2011/08/10
Phase 1
Withdrawn

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
AvPAK
50268-677
ORAL
9.9 mg in 1 1
4/12/2022
Method Pharmaceuticals, LLC
58657-164
ORAL
15 [iU] in 1 1
12/9/2023
Exeltis USA, Inc.
0642-7473
ORAL
9 mg in 1 1
2/14/2023
PureTek Corporation
59088-193
ORAL
30 mg in 1 1
1/11/2023
Carilion Materials Management
68151-2640
ORAL
22 mg in 1 1
4/1/2013
Trivia Pharmaceuticals, LLC
84781-012
ORAL
13.5 mg in 1 1
6/23/2025
Avion Pharmaceuticals, LLC
75854-313
ORAL
10 [iU] in 1 1
1/7/2021
WINDER LABORATORIES, LLC
75826-171
ORAL
6.75 mg in 1 1
1/31/2024
PureTek Corporation
59088-695
ORAL
10 mg in 1 1
12/13/2023
A-S Medication Solutions
50090-0356
ORAL
15 [iU] in 1 1
6/1/2017

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
Macutec Essentials
326524
Medicine
A
11/22/2019
Invite E Vitamin E Oil
18863
Pharmacare Laboratories Pty Ltd
Medicine
A
9/30/1991
Mega Lifesciences Lysine with Multivitamins Chewable Tablet
304262
Medicine
A
6/13/2018
Daily Multi Multivitamin
337216
Medicine
A
5/29/2020
1Above Reboot Orange & Mandarin
435637
Medicine
A
1/19/2024
Nature’s Way High Strength Adult Vita Gummies Triple Immune Support
406870
Pharmacare Laboratories Pty Ltd
Medicine
A
3/27/2023
ElementAll Diet
447331
Medicine
A
5/1/2024
Adult Vita Gummies Women's Multivitamin
461189
Pharmacare Laboratories Pty Ltd
Medicine
A
8/29/2024
Women`s Multi
460138
Medicine
A
8/20/2024
Daily Multi Multivitamin
443352
Medicine
A
3/7/2024

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
STRESS B COMPLEX WITH C AND E TAB
02008947
Tablet - Oral
30 UNIT / TAB
12/31/1993
VITAMIN E CAPSULES 800I.U. USP
vita health products inc
02041065
Capsule - Oral
800 UNIT / CAP
12/31/1995
29 MULTIVITAMINS + MINERALS - TAB
stanley pharmaceuticals, a division of vita health products inc.
02217775
Tablet - Oral
25 UNIT
10/18/1996
VITAMINS C PLUS E W.BETA CAROTENE AND SE
pharmetics (2011) inc
02208415
Tablet - Oral
200 UNIT
1/6/1997
FUSION AM FORMULA TAB
l & s research corporation
01961152
Tablet - Oral
30 UNIT / TAB
12/31/1993
ULTRAVITE FORTE WITH MINERALS 29
stanley pharmaceuticals, a division of vita health products inc.
01994379
Tablet - Oral
30 UNIT
12/31/1992
Z BEC TAB
whitehall-robins inc.
01932632
Tablet - Oral
45 UNIT
12/31/1994
STRESS B COMPLEX WITH C,E, ZINC AND COPPER
02008920
Tablet - Oral
30 UNIT
12/31/1993
SPECTRUM FORTE 29 TAB
ksl pharmaceuticals
01924877
Tablet - Oral
30 UNIT / TAB
12/31/1991
PARAMETTES ADULTS COMPLETE TAB
wyeth-ayerst canada inc.
02043092
Tablet - Oral
25 UNIT / TAB
12/31/1994

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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