NDC 49427-345-44 - PROIN ER

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 49427-345
Requested NDC: 49427-345-44
Package NDCs from labels: 49427-345-57, 49427-345-44
Manufacturer: Pegasus Laboratories, Inc.
Effective date: 2023-12-20
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
PROIN ER - Pegasus Laboratories, Inc.	Pegasus Laboratories, Inc.	2023-12-20	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49427-345-44	PROIN ER	90 in 1 BOTTLE	TABLET, EXTENDED RELEASE	90		2
49427-345-57	PROIN ER	30 in 1 BOTTLE	TABLET, EXTENDED RELEASE	30		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49427-345	PROIN ER (PHENYLPROPANOLAMINE HYDROCHLORIDE) TABLET, EXTENDED RELEASE [PEGASUS LABORATORIES, INC.]	2	2 package rows	20231221_c26843de-74ba-4a51-a18c-2d3bc0bcb07a.zip

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.