Mucinex D
Mucinex®D
Approved
Approval ID
98149172-3ec7-4212-9a37-5501bbfb5829
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 2, 2010
Manufacturers
FDA
Dispensing Solutions Inc.
DUNS: 066070785
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Guaifenesin and Pseudoephedrine Hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68258-3035
Application NumberNDA021585
Product Classification
M
Marketing Category
C73594
G
Generic Name
Guaifenesin and Pseudoephedrine Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateMarch 2, 2010
FDA Product Classification
INGREDIENTS (2)
GUAIFENESINActive
Quantity: 600 mg in 1 1
Code: 495W7451VQ
Classification: ACTIB
PSEUDOEPHEDRINE HYDROCHLORIDEActive
Quantity: 60 mg in 1 1
Code: 6V9V2RYJ8N
Classification: ACTIB