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Cialis

These highlights do not include all the information needed to use CIALIS safely and effectively. See full prescribing information for CIALIS. CIALIS (tadalafil) tablet, film coated for oral use Initial U.S. Approval: 2003

Approved
Approval ID

ebddb745-81f9-4b25-8739-b2886032ed26

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jul 28, 2009

Manufacturers
FDA

Rebel Distributors Corp.

DUNS: 118802834

Products 2

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

Tadalafil

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code21695-029
Application NumberNDA021368
Product Classification
M
Marketing Category
C73594
G
Generic Name
Tadalafil
Product Specifications
Route of AdministrationORAL
Effective DateApril 29, 2009
FDA Product Classification

INGREDIENTS (12)

TadalafilActive
Quantity: 20 mg in 1 1
Code: 742SXX0ICT
Classification: ACTIM
Hydroxypropyl celluloseInactive
Code: RFW2ET671P
Classification: IACT
HypromelloseInactive
Code: 3NXW29V3WO
Classification: IACT
Magnesium stearateInactive
Code: 70097M6I30
Classification: IACT
FERRIC OXIDE YELLOWInactive
Code: EX438O2MRT
Classification: IACT
Lactose monohydrateInactive
Code: EWQ57Q8I5X
Classification: IACT
Sodium lauryl sulfateInactive
Code: 368GB5141J
Classification: IACT
Cellulose, microcrystallineInactive
Code: OP1R32D61U
Classification: IACT
Croscarmellose sodiumInactive
Code: M28OL1HH48
Classification: IACT
TalcInactive
Code: 7SEV7J4R1U
Classification: IACT
Titanium dioxideInactive
Code: 15FIX9V2JP
Classification: IACT
TriacetinInactive
Code: XHX3C3X673
Classification: IACT

Tadalafil

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code21695-028
Application NumberNDA021368
Product Classification
M
Marketing Category
C73594
G
Generic Name
Tadalafil
Product Specifications
Route of AdministrationORAL
Effective DateApril 29, 2009
FDA Product Classification

INGREDIENTS (12)

Hydroxypropyl celluloseInactive
Code: RFW2ET671P
Classification: IACT
Magnesium stearateInactive
Code: 70097M6I30
Classification: IACT
TadalafilActive
Quantity: 10 mg in 1 1
Code: 742SXX0ICT
Classification: ACTIM
HypromelloseInactive
Code: 3NXW29V3WO
Classification: IACT
FERRIC OXIDE YELLOWInactive
Code: EX438O2MRT
Classification: IACT
Sodium lauryl sulfateInactive
Code: 368GB5141J
Classification: IACT
Lactose monohydrateInactive
Code: EWQ57Q8I5X
Classification: IACT
TalcInactive
Code: 7SEV7J4R1U
Classification: IACT
Cellulose, microcrystallineInactive
Code: OP1R32D61U
Classification: IACT
Titanium dioxideInactive
Code: 15FIX9V2JP
Classification: IACT
Croscarmellose sodiumInactive
Code: M28OL1HH48
Classification: IACT
TriacetinInactive
Code: XHX3C3X673
Classification: IACT

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