Cialis
- Product NDC
- 66336-566
- 11-digit product format
- 663360566
- Labeler code
- 66336
- Product ID
- 66336-566_02ba1d7c-aeef-452b-b748-6ecc1d88e340
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tadalafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Dispensing Solutions, Inc.
- Application
- NDA021368
- Marketing category
- NDA
- Marketing start
- 2003-11-26
- Marketing end
- 0000-00-00
- Substance
- TADALAFIL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66336-566-05 | Cialis | 5 in 1 BOTTLE | TABLET, FILM COATED | 5 | | 2 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| Tadalafil | ACTIVE INGREDIENT | 742SXX0ICT | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
| Tadalafil | ACTIVE MOIETY | 742SXX0ICT | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
| Cellulose, microcrystalline | INACTIVE INGREDIENT | OP1R32D61U | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
| Croscarmellose sodium | INACTIVE INGREDIENT | M28OL1HH48 | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
| Hydroxypropyl cellulose | INACTIVE INGREDIENT | RFW2ET671P | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
| Hypromelloses | INACTIVE INGREDIENT | 3NXW29V3WO | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
| Lactose monohydrate | INACTIVE INGREDIENT | EWQ57Q8I5X | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
| Magnesium stearate | INACTIVE INGREDIENT | 70097M6I30 | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
| Sodium lauryl sulfate | INACTIVE INGREDIENT | 368GB5141J | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
| Talc | INACTIVE INGREDIENT | 7SEV7J4R1U | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
| Titanium dioxide | INACTIVE INGREDIENT | 15FIX9V2JP | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
| Triacetin | INACTIVE INGREDIENT | XHX3C3X673 | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66336-566 | CIALIS (TADALAFIL) TABLET, FILM COATED [DISPENSING SOLUTIONS, INC.] | 2 | Legacy NDC, 1 package rows | 20120928_7178f6c0-bc15-49e1-bb65-1a8fe6f94191.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 66336-566-05 | 66336056605 | 5 in 1 BOTTLE | Historical |