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Latanoprost
Latanoprost - 0378-9645-32 - (latanoprost)
Drug Information of Latanoprost
| Product NDC: | 0378-9645 |
| Proprietary Name: | Latanoprost |
| Non Proprietary Name: | latanoprost |
| Active Ingredient(s): | 50 ug/mL & nbsp; latanoprost |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Latanoprost
| Product NDC: | 0378-9645 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201786 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110322 |
Package Information of Latanoprost
| Package NDC: | 0378-9645-32 |
| Package Description: | 1 BOTTLE in 1 CARTON (0378-9645-32) > 2.5 mL in 1 BOTTLE |
NDC Information of Latanoprost
| NDC Code | 0378-9645-32 |
| Proprietary Name | Latanoprost |
| Package Description | 1 BOTTLE in 1 CARTON (0378-9645-32) > 2.5 mL in 1 BOTTLE |
| Product NDC | 0378-9645 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | latanoprost |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110322 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | LATANOPROST |
| Strength Number | 50 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] |
