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Latisse
Latisse - 54868-6053-0 - (bimatoprost)
Drug Information of Latisse
| Product NDC: | 54868-6053 |
| Proprietary Name: | Latisse |
| Non Proprietary Name: | bimatoprost |
| Active Ingredient(s): | .3 mg/mL & nbsp; bimatoprost |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Latisse
| Product NDC: | 54868-6053 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022369 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090724 |
Package Information of Latisse
| Package NDC: | 54868-6053-0 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (54868-6053-0) > 3 mL in 1 BOTTLE, DROPPER |
NDC Information of Latisse
| NDC Code | 54868-6053-0 |
| Proprietary Name | Latisse |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (54868-6053-0) > 3 mL in 1 BOTTLE, DROPPER |
| Product NDC | 54868-6053 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bimatoprost |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20090724 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | BIMATOPROST |
| Strength Number | .3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] |
