Ofloxacin

Product NDC

70518-0308

11-digit product format

705180308

Labeler code

70518

Product ID

70518-0308_83830baf-1f03-3450-e053-2a91aa0a6ab0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ofloxacin

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

REMEDYREPACK INC.

Application

ANDA076407

Marketing category

ANDA

Marketing start

2017-03-10

Marketing end

0000-00-00

Substance

OFLOXACIN

Active strength

3 mg/mL

Pharmacologic classes

Quinolone Antimicrobial [EPC],Quinolones [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record