MedPath

Ravantage 45

Ravantage 45 (ractopamine hydrochloride Type A medicated article)

Approved
Approval ID

2c1155f4-dd52-4627-acff-ab195deca9d9

Product Type

OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL

Effective Date

Apr 1, 2025

Manufacturers
FDA

Huvepharma, Inc

DUNS: 619153559

Products 1

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

ractopamine hydrochloride

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code23243-5278
Application NumberANADA200768
Product Classification
M
Marketing Category
C73583
G
Generic Name
ractopamine hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateApril 1, 2025
FDA Product Classification

INGREDIENTS (4)

CASTOR OILInactive
Code: D5340Y2I9G
Classification: IACT
povidoneInactive
Code: FZ989GH94E
Classification: IACT
CORN COBInactive
Code: XXP8V4H4NY
Classification: IACT
ractopamine hydrochlorideActive
Quantity: 45.4 g in 0.45 kg
Code: 309G9J93TP
Classification: ACTIB

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Ravantage 45 - FDA Drug Approval Details