NDC properties for "Cialis 10 MG Oral Tablet" (RxCUI 402096)
About this data
The tables show NDC propoerties for Cialis 10 MG Oral Tablet with the RxCUI 402096
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product
Details for Cialis 10 MG Oral Tablet (RxCUI 402096)
| MMSL_CODE | BD9139 |
|---|---|
| NDA | NDA021368 |
| RxCUI | 402096 |
| SPL_SET_ID | 0e747223-2740-4e45-9bef-ae5f7798064a |
| SPL_SET_ID | 6a8621eb-7415-42a6-9432-630751d34c6b |
| SPL_SET_ID | bcd8f8ab-81a2-4891-83db-24a0b0e25895 |
| SPL_SET_ID | ebddb745-81f9-4b25-8739-b2886032ed26 |
| SPL_SET_ID | ee053358-9746-4475-9d3d-ca83ea84c125 |
| Prescribable Synonym | Cialis 10 MG Oral Tablet |
| RXNAV_STR | Cialis 10 MG Oral Tablet |
| RxNorm Name | tadalafil 10 MG Oral Tablet [Cialis] |
| RxNorm Synonym | Cialis 10 MG Oral Tablet |
| Related queries | Interactions (for RxCUI 402096) |
NDC Properties
NDC Item 00002446330
| NDC 9 | 0002-4463 |
|---|---|
| NDC 10 | 0002-4463-30 |
| NDC Item | 00002446330 |
| Packaging | 30 TABLET, FILM COATED in 1 BOTTLE (0002-4463-30) |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 486344 |
| Imprint code | C;10 |
| Labeler | Eli Lilly and Company |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2003-11-26 |
| Marketing status | ACTIVE |
| NDA | NDA021368 |
| Score | 1 |
| Shapetext | almond |
| Shape | C48345 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0002-4463 |
NDC Item 68071060608
| NDC 9 | 68071-606 |
|---|---|
| NDC 10 | 68071-606-08 |
| NDC Item | 68071060608 |
| Related queries | Properties for NDC 9 68071-606 |
NDC Item 68071060610
| NDC 9 | 68071-606 |
|---|---|
| NDC 10 | 68071-606-10 |
| NDC Item | 68071060610 |
| Related queries | Properties for NDC 9 68071-606 |
NDC Item 00002446330
| NDC 9 | 0002-4463 |
|---|---|
| NDC 10 | 0002-4463-30 |
| NDC Item | 00002446330 |
| Packaging | 30 TABLET, FILM COATED in 1 BOTTLE (0002-4463-30) |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 486344 |
| Imprint code | C;10 |
| Labeler | Eli Lilly and Company |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2003-11-26 |
| Marketing status | ACTIVE |
| NDA | NDA021368 |
| Score | 1 |
| Shapetext | almond |
| Shape | C48345 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0002-4463 |
NDC Item 68071060608
| NDC 9 | 68071-606 |
|---|---|
| NDC 10 | 68071-606-08 |
| NDC Item | 68071060608 |
| Related queries | Properties for NDC 9 68071-606 |
NDC Item 68071060610
| NDC 9 | 68071-606 |
|---|---|
| NDC 10 | 68071-606-10 |
| NDC Item | 68071060610 |
| Related queries | Properties for NDC 9 68071-606 |
NDC Item 00002446330
| NDC 9 | 0002-4463 |
|---|---|
| NDC 10 | 0002-4463-30 |
| NDC Item | 00002446330 |
| Packaging | 30 TABLET, FILM COATED in 1 BOTTLE (0002-4463-30) |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 486344 |
| Imprint code | C;10 |
| Labeler | Eli Lilly and Company |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2003-11-26 |
| Marketing status | ACTIVE |
| NDA | NDA021368 |
| Score | 1 |
| Shapetext | almond |
| Shape | C48345 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0002-4463 |
NDC Item 68071060608
| NDC 9 | 68071-606 |
|---|---|
| NDC 10 | 68071-606-08 |
| NDC Item | 68071060608 |
| Related queries | Properties for NDC 9 68071-606 |
NDC Item 68071060610
| NDC 9 | 68071-606 |
|---|---|
| NDC 10 | 68071-606-10 |
| NDC Item | 68071060610 |
| Related queries | Properties for NDC 9 68071-606 |