NEOMYCIN SULFATE

Product NDC

51991-738

11-digit product format

519910738

Labeler code

51991

Product ID

51991-738_af6c619c-40ee-4fcb-b8ab-ba50ba6990fa

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

NEOMYCIN SULFATE

Dosage form

TABLET

Route

ORAL

Labeler

Breckenridge Pharmaceutical, Inc.

Application

ANDA065468

Marketing category

ANDA

Marketing start

2011-01-03

Marketing end

2020-04-30

Substance

NEOMYCIN SULFATE

Active strength

350 mg/1

Pharmacologic classes

Aminoglycoside Antibacterial [EPC],Aminoglycosides [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record