Triprolidine Hydrochloride

Product NDC

69784-102

11-digit product format

697840102

Labeler code

69784

Product ID

69784-102_9f88fecd-3926-4513-9f23-a4bcbec0b6fb

Type

HUMAN OTC DRUG

Nonproprietary name

TRIPROLIDINE HYDROCHLORIDE

Dosage form

LIQUID

Route

ORAL

Labeler

Woodward Pharma Services LLC

Application

part341

Marketing category

OTC MONOGRAPH FINAL

Marketing start

2016-10-10

Marketing end

0000-00-00

Substance

TRIPROLIDINE HYDROCHLORIDE

Active strength

1 mg/mL

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record