NDC properties for "tetracaine HCl 2 % Topical Cream" (RxCUI 1543158)
About this data
The tables show NDC propoerties for tetracaine HCl 2 % Topical Cream with the RxCUI 1543158
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 tetracaine HCl 2 % Topical Cream (RxCUI 1543158)
| MMSL_CODE | CD8557 |
|---|---|
| RxCUI | 1543158 |
| SNOMEDCT | 370306008 |
| SPL_SET_ID | 3c1e3a1d-f42b-499d-a445-1d1d3dd26c19 |
| SPL_SET_ID | 6e0e3594-0c69-495e-9972-13af2773c88d |
| SPL_SET_ID | 90f644b4-faa2-4f54-865a-44ccdab99ad3 |
| SPL_SET_ID | bb67a8d2-8799-4672-ac4a-a9124f1f543f |
| SPL_SET_ID | be19e1aa-0dae-4534-8cff-2af13347e963 |
| Prescribable Synonym | tetracaine HCl 2 % Topical Cream |
| RXNAV_STR | tetracaine hydrochloride 20 MG/ML Topical Cream |
| RxNorm Name | tetracaine hydrochloride 20 MG/ML Topical Cream |
| RxNorm Synonym | tetracaine HCl 2 % Topical Cream |
| Related queries | Interactions (for RxCUI 1543158) |
NDC Properties
NDC Item 54723031003
| NDC 9 | 54723-310 |
|---|---|
| NDC 10 | 54723-310-03 |
| NDC Item | 54723031003 |
| Packaging | 3000 mg in 1 PACKET (54723-310-03) |
| FDA SPL set id | 807826 |
| Labeler | Sambria Pharmaceuticals, Inc. |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2016-02-01 |
| Marketing status | ACTIVE |
| OTC_MONOGRAPH_DRUG | M017 |
| Related queries | Properties for NDC 9 54723-310 |
NDC Item 54723031004
| NDC 9 | 54723-310 |
|---|---|
| NDC 10 | 54723-310-04 |
| NDC Item | 54723031004 |
| Packaging | 1500 mg in 1 PACKAGE (54723-310-04) |
| FDA SPL set id | 807826 |
| Labeler | Sambria Pharmaceuticals, Inc. |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2016-02-01 |
| Marketing status | ACTIVE |
| OTC_MONOGRAPH_DRUG | M017 |
| Related queries | Properties for NDC 9 54723-310 |
NDC Item 54723031003
| NDC 9 | 54723-310 |
|---|---|
| NDC 10 | 54723-310-03 |
| NDC Item | 54723031003 |
| Packaging | 3000 mg in 1 PACKET (54723-310-03) |
| FDA SPL set id | 807826 |
| Labeler | Sambria Pharmaceuticals, Inc. |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2016-02-01 |
| Marketing status | ACTIVE |
| OTC_MONOGRAPH_DRUG | M017 |
| Related queries | Properties for NDC 9 54723-310 |
NDC Item 54723031004
| NDC 9 | 54723-310 |
|---|---|
| NDC 10 | 54723-310-04 |
| NDC Item | 54723031004 |
| Packaging | 1500 mg in 1 PACKAGE (54723-310-04) |
| FDA SPL set id | 807826 |
| Labeler | Sambria Pharmaceuticals, Inc. |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2016-02-01 |
| Marketing status | ACTIVE |
| OTC_MONOGRAPH_DRUG | M017 |
| Related queries | Properties for NDC 9 54723-310 |