FDA Product

Nadolol

Product approved by U.S. Food and Drug Administration (US)

Basic Information

Product Name

Nadolol

FDA Product Code

67787-347

Regulatory Information

NDC Product Code

67787-347

Application Number

ANDA203455

Marketing Category

C73584

Effective Date

August 21, 2017

Territorial Authority

USA

FDA Title

Rx Only

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

2

Company Information

ManufacturerInvaGen Pharmaceuticals Inc.

DUNS Number

165104469

Active Ingredients

LACTOSE MONOHYDRATE

Code: EWQ57Q8I5X

Class Code: IACT

POVIDONE, UNSPECIFIED

Code: FZ989GH94E

Class Code: IACT

MICROCRYSTALLINE CELLULOSE

Code: OP1R32D61U

Class Code: IACT

Quantity: 20 mg in 1 1

Code: FEN504330V

Class Code: ACTIB

D&C YELLOW NO. 10

Code: 35SW5USQ3G

Class Code: IACT

MAGNESIUM STEARATE

Code: 70097M6I30

Class Code: IACT

CROSCARMELLOSE SODIUM

Code: M28OL1HH48

Class Code: IACT

Active Moieties

NADOLOL

Code: FEN504330V

© Copyright 2025. All Rights Reserved by MedPath

Home Terms & Conditions Privacy Policy