FDA.reportPublic FDA data

NDC 49427-922-50 - PhenylPro 75

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
49427-922
Requested NDC
49427-922-50
Package NDCs from labels
49427-922-48, 49427-922-50
Manufacturer
Pegasus Laboratories, Inc. | Cheng Fong Chemical Co Ltd
Effective date
2025-12-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PhenylPro 75 - Pegasus Laboratories, Inc. | Cheng Fong Chemical Co LtdPegasus Laboratories, Inc. | Cheng Fong Chemical Co Ltd2025-12-29PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49427-922-48PhenylPro 7560 in 1 BOTTLETABLET, CHEWABLE602
49427-922-50PhenylPro 75180 in 1 BOTTLETABLET, CHEWABLE1802

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49427-922PHENYLPRO 75 (PHENYLPROPANOLOAMINE HYDROCHLORIDE) TABLET, CHEWABLE [PEGASUS LABORATORIES, INC.]12 package rows20250424_070aa5ff-efd6-4114-86a0-34baf5e646b2.zip

Reported adverse events (FAERS/openFDA)#

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