NDC properties for "Zylet (loteprednol etabonate 0.5 % / tobramycin 0.3 % ) Ophthalmic Suspension" (RxCUI 545259)
About this data
The tables show NDC propoerties for Zylet (loteprednol etabonate 0.5 % / tobramycin 0.3 % ) Ophthalmic Suspension with the RxCUI 545259
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 Zylet (loteprednol etabonate 0.5 % / tobramycin 0.3 % ) Ophthalmic Suspension (RxCUI 545259)
| MMSL_CODE | BD13265 |
|---|---|
| NDA | NDA050804 |
| RxCUI | 545259 |
| SPL_SET_ID | 3dd9b060-5355-404d-bdf1-09ee8b52a9f5 |
| Prescribable Synonym | Zylet 0.5 % / 0.3 % Ophthalmic Suspension |
| RXNAV_STR | Zylet (loteprednol etabonate 0.5 % / tobramycin 0.3 % ) Ophthalmic Suspension |
| RxNorm Name | loteprednol etabonate 5 MG/ML / tobramycin 3 MG/ML Ophthalmic Suspension [Zylet] |
| RxNorm Synonym | Zylet (loteprednol etabonate 0.5 % / tobramycin 0.3 % ) Ophthalmic Suspension |
| RxNorm Synonym | Zylet (loteprednol etabonate 5 MG / tobramycin 3 MG) per ML Ophthalmic Suspension |
| Related queries | Interactions (for RxCUI 545259) |
NDC Properties
NDC Item 24208035801
| NDC 9 | 24208-358 |
|---|---|
| NDC 10 | 24208-358-01 |
| NDC Item | 24208035801 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-01) / 1 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 595435 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-12-14 |
| Marketing status | ACTIVE |
| NDA | NDA050804 |
| Related queries | Properties for NDC 9 24208-358 |
NDC Item 24208035805
| NDC 9 | 24208-358 |
|---|---|
| NDC 10 | 24208-358-05 |
| NDC Item | 24208035805 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-05) / 5 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 595435 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-12-14 |
| Marketing status | ACTIVE |
| NDA | NDA050804 |
| Related queries | Properties for NDC 9 24208-358 |
NDC Item 24208035810
| NDC 9 | 24208-358 |
|---|---|
| NDC 10 | 24208-358-10 |
| NDC Item | 24208035810 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-10) / 10 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 595435 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-12-14 |
| Marketing status | ACTIVE |
| NDA | NDA050804 |
| Related queries | Properties for NDC 9 24208-358 |
NDC Item 24208035801
| NDC 9 | 24208-358 |
|---|---|
| NDC 10 | 24208-358-01 |
| NDC Item | 24208035801 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-01) / 1 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 595435 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-12-14 |
| Marketing status | ACTIVE |
| NDA | NDA050804 |
| Related queries | Properties for NDC 9 24208-358 |
NDC Item 24208035805
| NDC 9 | 24208-358 |
|---|---|
| NDC 10 | 24208-358-05 |
| NDC Item | 24208035805 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-05) / 5 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 595435 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-12-14 |
| Marketing status | ACTIVE |
| NDA | NDA050804 |
| Related queries | Properties for NDC 9 24208-358 |
NDC Item 24208035810
| NDC 9 | 24208-358 |
|---|---|
| NDC 10 | 24208-358-10 |
| NDC Item | 24208035810 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-10) / 10 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 595435 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-12-14 |
| Marketing status | ACTIVE |
| NDA | NDA050804 |
| Related queries | Properties for NDC 9 24208-358 |
NDC Item 24208035801
| NDC 9 | 24208-358 |
|---|---|
| NDC 10 | 24208-358-01 |
| NDC Item | 24208035801 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-01) / 1 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 595435 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-12-14 |
| Marketing status | ACTIVE |
| NDA | NDA050804 |
| Related queries | Properties for NDC 9 24208-358 |
NDC Item 24208035805
| NDC 9 | 24208-358 |
|---|---|
| NDC 10 | 24208-358-05 |
| NDC Item | 24208035805 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-05) / 5 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 595435 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-12-14 |
| Marketing status | ACTIVE |
| NDA | NDA050804 |
| Related queries | Properties for NDC 9 24208-358 |
NDC Item 24208035810
| NDC 9 | 24208-358 |
|---|---|
| NDC 10 | 24208-358-10 |
| NDC Item | 24208035810 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-10) / 10 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 595435 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-12-14 |
| Marketing status | ACTIVE |
| NDA | NDA050804 |
| Related queries | Properties for NDC 9 24208-358 |