Gentamicin Sulfate

Product NDC

50436-6754

11-digit product format

504366754

Labeler code

50436

Product ID

50436-6754_dfeb350f-80e2-412c-8363-8e9beee7c29e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Gentamicin Sulfate

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

Unit Dose Services

Application

ANDA064048

Marketing category

ANDA

Marketing start

1994-05-11

Marketing end

0000-00-00

Substance

GENTAMICIN SULFATE

Active strength

3 mg/mL

Pharmacologic classes

Aminoglycoside Antibacterial [EPC],Aminoglycosides [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record