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 | 582712 |
Labeler | Endo Pharmaceuticals 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 | 582712 |
Labeler | Endo Pharmaceuticals 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 | 582712 |
Labeler | Endo Pharmaceuticals 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 | 582712 |
Labeler | Endo Pharmaceuticals 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 |