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ALBUTEROL SULFATE

1175 ALBUTEROL (VENTOLIN)

Approved
Approval ID

87747f82-9008-ab34-e053-2995a90a6808

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Apr 26, 2019

Manufacturers
FDA

H.J. Harkins Company, Inc.

DUNS: 147681894

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

ALBUTEROL SULFATE

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code76519-1175
Application NumberNDA020983
Product Classification
M
Marketing Category
C73605
G
Generic Name
ALBUTEROL SULFATE
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateApril 26, 2019
FDA Product Classification

INGREDIENTS (1)

ALBUTEROL SULFATEActive
Quantity: 90 ug in 1 g
Code: 021SEF3731
Classification: ACTIM

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ALBUTEROL SULFATE - FDA Drug Approval Details