NDC properties for "5000 MG Testim 0.01 MG/MG Topical Gel" (RxCUI 1597132)
About this data
The tables show NDC propoerties for 5000 MG Testim 0.01 MG/MG Topical Gel with the RxCUI 1597132
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 5000 MG Testim 0.01 MG/MG Topical Gel (RxCUI 1597132)
| MMSL_CODE | BD22847 |
|---|---|
| MMSL_CODE | BN59775 |
| NDA | NDA021454 |
| RxCUI | 1597132 |
| SPL_SET_ID | 0d90cadf-d579-47bf-b655-7e9d3bd1cabe |
| SPL_SET_ID | 48f8aa83-e043-41b8-9a20-dbb098045895 |
| SPL_SET_ID | 9f2aae1f-898d-4955-be31-678e0cf85395 |
| VUID | 4029617 |
| Prescribable Synonym | Testim 1 % (50 MG / 5GM) Transdermal Gel |
| RXNAV_STR | 5000 MG Testim 0.01 MG/MG Topical Gel |
| RxNorm Name | 5000 MG testosterone 0.01 MG/MG Topical Gel [Testim] |
| RxNorm Synonym | 5000 MG Testim 0.01 MG/MG Topical Gel |
| RxNorm Synonym | Testim 1 % (50 MG) Transdermal Gel, 5 GM |
| Related queries | Interactions (for RxCUI 1597132) |
NDC Properties
NDC Item 66887000101
| NDC 9 | 66887-001 |
|---|---|
| NDC 10 | 66887-001-01 |
| NDC Item | 66887000101 |
| DCSA | CIII |
| FDA SPL set id | 809415 |
| Labeler | Endo USA, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2002-10-31 |
| Marketing status | ACTIVE |
| NDA | NDA021454 |
| Related queries | Properties for NDC 9 66887-001 |
NDC Item 66887000105
| NDC 9 | 66887-001 |
|---|---|
| NDC 10 | 66887-001-05 |
| NDC Item | 66887000105 |
| Packaging | 30 TUBE in 1 CARTON (66887-001-05) / 5 g in 1 TUBE |
| DCSA | CIII |
| FDA SPL set id | 809415 |
| Labeler | Endo USA, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2002-10-31 |
| Marketing status | ACTIVE |
| NDA | NDA021454 |
| Related queries | Properties for NDC 9 66887-001 |
NDC Item 66887000101
| NDC 9 | 66887-001 |
|---|---|
| NDC 10 | 66887-001-01 |
| NDC Item | 66887000101 |
| DCSA | CIII |
| FDA SPL set id | 809415 |
| Labeler | Endo USA, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2002-10-31 |
| Marketing status | ACTIVE |
| NDA | NDA021454 |
| Related queries | Properties for NDC 9 66887-001 |
NDC Item 66887000105
| NDC 9 | 66887-001 |
|---|---|
| NDC 10 | 66887-001-05 |
| NDC Item | 66887000105 |
| Packaging | 30 TUBE in 1 CARTON (66887-001-05) / 5 g in 1 TUBE |
| DCSA | CIII |
| FDA SPL set id | 809415 |
| Labeler | Endo USA, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2002-10-31 |
| Marketing status | ACTIVE |
| NDA | NDA021454 |
| Related queries | Properties for NDC 9 66887-001 |