sunmark loratadine d

Product NDC

49348-183

11-digit product format

493480183

Labeler code

49348

Product ID

49348-183_12eb2874-467b-43e4-aab2-0311fc7da144

Type

HUMAN OTC DRUG

Nonproprietary name

Loratadine, Pseudoephedrine

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

McKesson

Application

ANDA076050

Marketing category

ANDA

Marketing start

2012-03-06

Marketing end

2019-08-31

Substance

LORATADINE; PSEUDOEPHEDRINE SULFATE

Active strength

5 mg/1; mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record