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Penicillin V Potassium

Penicillin-VKPenicillin V Potassium Tablets, USP500 mg (800,000 Units)

Approved
Approval ID

4cdff640-870e-4de8-885b-0669bfde518d

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 9, 2011

Manufacturers
FDA

Rebel Distributors Corp

DUNS: 118802834

Products 1

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

Penicillin V Potassium

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code21695-318
Application NumberANDA062935
Product Classification
M
Marketing Category
C73584
G
Generic Name
Penicillin V Potassium
Product Specifications
Route of AdministrationORAL
Effective DateDecember 8, 2006
FDA Product Classification

INGREDIENTS (7)

MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
POVIDONEInactive
Code: FZ989GH94E
Classification: IACT
POLYETHYLENE GLYCOLInactive
Code: 3WJQ0SDW1A
Classification: IACT
LACTOSEInactive
Code: J2B2A4N98G
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
PENICILLIN V POTASSIUMActive
Quantity: 500 mg in 1 1
Code: 146T0TU1JB
Classification: ACTIB

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Penicillin V Potassium - FDA Drug Approval Details