Trimethoprim

Product NDC

50268-775

11-digit product format

502680775

Labeler code

50268

Product ID

50268-775_7e7c1773-8851-74d1-e053-2a91aa0a490e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Trimethoprim

Dosage form

TABLET

Route

ORAL

Labeler

AvPAK

Application

ANDA070049

Marketing category

ANDA

Marketing start

2013-07-31

Marketing end

2019-03-31

Substance

TRIMETHOPRIM

Active strength

100 mg/1

Pharmacologic classes

Dihydrofolate R

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record