MedPath

Sodium ascorbate

Generic Name
Sodium ascorbate
Brand Names
Irospan 24/6 Kit, Mega-C, Moviprep, Plenvu, Tandem Plus
Drug Type
Small Molecule
Chemical Formula
C6H7NaO6
CAS Number
134-03-2
Unique Ingredient Identifier
S033EH8359

Overview

No overview information available.

Indication

No indication information available.

Associated Conditions

  • Common Cold
  • Cough
  • Fever
  • Flu caused by Influenza
  • Hoarseness
  • Pain
  • Throat irritation

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2021/03/15
Phase 1
Recruiting
2005/09/28
Phase 1
Completed
Jeanne Drisko, MD, CNS, FACN

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Cameron Pharmaceuticals
42494-432
ORAL
60 mg in 1 1
9/18/2023
PureTek Corporation
59088-112
ORAL
200 mg in 1 1
1/11/2023
WINDER LABORATORIES, LLC
75826-171
ORAL
36 mg in 1 1
1/31/2024
PureTek Corporation
59088-695
ORAL
36 mg in 1 1
12/13/2023
A-S Medication Solutions
50090-4475
ORAL
36 mg in 1 1
4/3/2020
WINDER LABORATORIES, LLC
75826-170
ORAL
36 mg in 1 1
1/31/2024
PureTek Corporation
59088-015
ORAL
36 mg in 1 1
3/3/2025
PureTek Corporation
59088-107
ORAL
36 mg in 1 1
1/31/2023
Cameron Pharmaceuticals
42494-433
ORAL
60 mg in 1 1
9/18/2023
PureTek Corporation
59088-018
ORAL
36 mg in 1 1
5/15/2025

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
ENTRESTO FILM COATED TABLET 200MG
SIN14949P
TABLET, FILM COATED
200mg
2/12/2016
ENTRESTO FILM COATED TABLET 50MG
SIN14947P
TABLET, FILM COATED
50mg
2/12/2016
SOLUVIT N FOR INFUSION
SIN05209P
INJECTION, POWDER, FOR SOLUTION
113mg/vial
11/14/1990

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.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
VITAMINE C 100MG TAB MASTICABLE
bio vita
00742252
Tablet - Oral
57 MG / TAB
12/31/1987
VIT C TAB 500MG
albi naturals
00571326
Tablet - Oral
277.5 MG
12/31/1982
VITAMINE C TAB 250MG
distributions multi-pro inc.
00585378
Tablet - Oral
114 MG
12/31/1984
TWIN PRO POWDER VANILLA
twin laboratories inc.
02014149
Powder - Oral
21 MG / 71.35 G
12/31/1995
CHEWABLE VITAMIN C 250MG
randle labs inc.
00662097
Tablet - Oral
121.36 MG / TAB
12/31/1987
CHEWABLE VITAMIN C 500MG TAB
hall laboratories, ltd.
00608394
Tablet - Oral
227 MG
12/31/1987
CHEWABLE VIT C 100MG
bioforce canada inc.
01983903
Tablet - Oral
50 MG / TAB
12/31/1994
VITAMIN C TAB 100MG
albi naturals
00483060
Tablet - Oral
45 MG
12/31/1979
VITAMIN C TAB 500MG CHEWABLE
country health laboratories ltd.
00571563
Tablet - Oral
277.5 MG / TAB
12/31/1985
PRENAVITE FORTE TABLETS
roberts pharmaceutical canada inc.
02063182
Tablet - Oral
100 MG / TAB
12/31/1995

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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