LEVOBUNOLOL HYDROCHLORIDE

Product NDC

60758-063

11-digit product format

607580063

Labeler code

60758

Product ID

60758-063_4c9f95ab-89a1-401d-870e-ba728a385927

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

levobunolol hydrochloride

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

Pacific Pharma, Inc.

Application

NDA019814

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

1997-07-15

Marketing end

2021-01-31

Substance

LEVOBUNOLOL HYDROCHLORIDE

Active strength

3 mg/mL

Pharmacologic classes

Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record