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LATANOPROST
LATANOPROST - 17478-625-12 - (LATANOPROST)
Drug Information of LATANOPROST
| Product NDC: | 17478-625 |
| Proprietary Name: | LATANOPROST |
| Non Proprietary Name: | LATANOPROST |
| Active Ingredient(s): | 50 ug/mL & nbsp; LATANOPROST |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LATANOPROST
| Product NDC: | 17478-625 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090887 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120701 |
Package Information of LATANOPROST
| Package NDC: | 17478-625-12 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (17478-625-12) > 2.5 mL in 1 BOTTLE, DROPPER |
NDC Information of LATANOPROST
| NDC Code | 17478-625-12 |
| Proprietary Name | LATANOPROST |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (17478-625-12) > 2.5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 17478-625 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LATANOPROST |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20120701 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn, Inc. |
| Substance Name | LATANOPROST |
| Strength Number | 50 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] |
