MedPath

Rattus norvegicus skin

Generic Name
Rattus norvegicus skin
Drug Type
Biotech
Unique Ingredient Identifier
Y69HPD48AI

Overview

Rattus norvegicus skin or pelt is used in allergenic testing.

Background

Rattus norvegicus skin or pelt 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

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Nelco Laboratories, Inc.
36987-1111
INTRADERMAL, SUBCUTANEOUS
0.1 g in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-1108
INTRADERMAL, SUBCUTANEOUS
20000 [PNU] in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-1106
INTRADERMAL, SUBCUTANEOUS
10000 [PNU] in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-1112
INTRADERMAL, SUBCUTANEOUS
0.1 g in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-1110
INTRADERMAL, SUBCUTANEOUS
0.05 g in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-1109
INTRADERMAL, SUBCUTANEOUS
0.05 g in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-1105
INTRADERMAL, SUBCUTANEOUS
10000 [PNU] in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-1107
INTRADERMAL, SUBCUTANEOUS
20000 [PNU] in 1 mL
12/3/2009

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.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.
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