Gentak

Product NDC

70518-0633

11-digit product format

705180633

Labeler code

70518

Product ID

70518-0633_865ff925-caa8-7455-e053-2a91aa0aa309

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Gentamicin Sulfate

Dosage form

OINTMENT

Route

OPHTHALMIC

Labeler

REMEDYREPACK INC.

Application

ANDA064093

Marketing category

ANDA

Marketing start

2017-07-24

Marketing end

0000-00-00

Substance

GENTAMICIN SULFATE

Active strength

3 mg/g

Pharmacologic classes

Aminoglycoside Antibacterial [EPC],Aminoglycosides [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record