Tobramycin

Product NDC

0703-9402

11-digit product format

007039402

Labeler code

0703

Product ID

0703-9402_6c2f7dfc-32de-4609-9065-baf94d064b32

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tobramycin

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Teva Parenteral Medicines, Inc.

Application

ANDA063100

Marketing category

ANDA

Marketing start

1992-02-01

Marketing end

2019-11-30

Substance

TOBRAMYCIN SULFATE

Active strength

40 mg/mL

Pharmacologic classes

Aminoglycoside Antibacterial [EPC],Aminoglycosides [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record