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Pliaglis

These highlights do not include all the information needed to use PLIAGLIS safely and effectively. See full prescribing information for PLIAGLIS. PLIAGLIS (lidocaine and tetracaine) cream, for topical use Initial U.S. Approval: 2006

Approved
Approval ID

8a1b2553-ce65-4557-b33d-cb3dd2a307fa

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Aug 19, 2020

Manufacturers
FDA

Oba Pharmaceuticals, Inc.

DUNS: 117380833

Products 1

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

lidocaine and tetracaine

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code73575-009
Application NumberNDA021717
Product Classification
M
Marketing Category
C73594
G
Generic Name
lidocaine and tetracaine
Product Specifications
Route of AdministrationTOPICAL
Effective DateAugust 19, 2020
FDA Product Classification

INGREDIENTS (9)

tetracaineActive
Quantity: 70 mg in 1 g
Code: 0619F35CGV
Classification: ACTIB
ANHYDROUS DIBASIC CALCIUM PHOSPHATEInactive
Code: L11K75P92J
Classification: IACT
PROPYLPARABENInactive
Code: Z8IX2SC1OH
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT
POLYVINYL ALCOHOL, UNSPECIFIEDInactive
Code: 532B59J990
Classification: IACT
METHYLPARABENInactive
Code: A2I8C7HI9T
Classification: IACT
lidocaineActive
Quantity: 70 mg in 1 g
Code: 98PI200987
Classification: ACTIB
SORBITAN MONOPALMITATEInactive
Code: 77K6Z421KU
Classification: IACT

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Pliaglis - FDA Drug Approval Details