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Octocaine 50

Octocaine(Lidocaine hydrochloride and epinephrine injection, USP)

Approved
Approval ID

7dfc8c0e-3d4d-4142-8e99-df833702cb9b

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 15, 2011

Manufacturers
FDA

Septodont

DUNS: 627058738

Products 1

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

Lidocaine Hydrochloride and Epinephrine Bitartrate

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0362-9010
Application NumberANDA088389
Product Classification
M
Marketing Category
C73584
G
Generic Name
Lidocaine Hydrochloride and Epinephrine Bitartrate
Product Specifications
Route of AdministrationSUBCUTANEOUS
Effective DateDecember 15, 2011
FDA Product Classification

INGREDIENTS (7)

Lidocaine HydrochlorideActive
Quantity: 20 mg in 1 mL
Code: V13007Z41A
Classification: ACTIB
Potassium MetabisulfiteInactive
Quantity: 1.2 mg in 1 mL
Code: 65OE787Q7W
Classification: IACT
Epinephrine BitartrateActive
Quantity: 0.02 mg in 1 mL
Code: 30Q7KI53AK
Classification: ACTIM
Edetate DisodiumInactive
Quantity: 0.25 mg in 1 mL
Code: 7FLD91C86K
Classification: IACT
Sodium ChlorideInactive
Quantity: 6.5 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT
Sodium HydroxideInactive
Code: 55X04QC32I
Classification: IACT
WaterInactive
Code: 059QF0KO0R
Classification: IACT

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Octocaine 50 - FDA Drug Approval Details