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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

NDC Product Code49427-922
Application NumberNADA141324
Marketing CategoryC73593
Route of AdministrationORAL
Effective DateApril 21, 2025
Generic Namephenylpropanoloamine hydrochloride

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 Approval | MedPath