MedPath

PhenylPro 75

Approved
Approval ID

070aa5ff-efd6-4114-86a0-34baf5e646b2

Product Type

PRESCRIPTION ANIMAL DRUG LABEL

Effective Date

Apr 21, 2025

Manufacturers
FDA

Pegasus Laboratories, Inc.

DUNS: 108454760

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

phenylpropanoloamine hydrochloride

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code49427-922
Application NumberNADA141324
Product Classification
M
Marketing Category
C73593
G
Generic Name
phenylpropanoloamine hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateApril 21, 2025
FDA Product Classification

INGREDIENTS (9)

SORBITOLInactive
Code: 506T60A25R
Classification: IACT
WHEYInactive
Code: 8617Z5FMF6
Classification: IACT
DIBASIC CALCIUM PHOSPHATE DIHYDRATEInactive
Code: O7TSZ97GEP
Classification: IACT
GARLICInactive
Code: V1V998DC17
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
SOY PROTEINInactive
Code: R44IWB3RN5
Classification: IACT
YEASTInactive
Code: 3NY3SM6B8U
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
PHENYLPROPANOLAMINE HYDROCHLORIDEActive
Quantity: 75 1 in 1 1
Code: 8D5I63UE1Q
Classification: ACTIB

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PhenylPro 75 - FDA Drug Approval Details