MedPath

Saccharomyces cerevisiae

Generic Name
Saccharomyces cerevisiae
Drug Type
Biotech
CAS Number
68876-77-7
Unique Ingredient Identifier
978D8U419H

Overview

Saccharomyces cerevisiae is a fungus which can provoke allergic reactions. Saccharomyces cerevisiae is used in allergenic testing.

Indication

No indication information available.

Associated Conditions

No associated conditions information available.

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2021/12/08
Phase 1
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Nelco Laboratories, Inc.
36987-1661
INTRADERMAL, SUBCUTANEOUS
0.1 g in 1 mL
12/9/2009
Nelco Laboratories, Inc.
36987-1659
INTRADERMAL, SUBCUTANEOUS
0.05 g in 1 mL
12/9/2009
Deseret Biologicals, Inc.
43742-2218
ORAL
10 [hp_X] in 1 mL
5/27/2025
Nutritional Specialties, Inc.
83027-0123
ORAL
16 [hp_X] in 1 mL
5/15/2025
Antigen Laboratories, Inc.
49288-0004
SUBCUTANEOUS, INTRADERMAL
0.0067 g in 1 mL
11/17/2009
Nelco Laboratories, Inc.
36987-2093
SUBCUTANEOUS, INTRADERMAL
20000 [PNU] in 1 mL
12/14/2009
Nelco Laboratories, Inc.
36987-2092
SUBCUTANEOUS, INTRADERMAL
10000 [PNU] in 1 mL
12/14/2009
King Bio Inc.
57955-0762
ORAL
12 [hp_X] in 59 mL
5/20/2025
King Bio Inc.
57955-4809
ORAL
12 [hp_X] in 118 mL
5/2/2025
Nelco Laboratories, Inc.
36987-2091
SUBCUTANEOUS, INTRADERMAL
10000 [PNU] in 1 mL
12/14/2009

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.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

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.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.