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LUMIGAN
LUMIGAN - 0023-3205-08 - (bimatoprost)
Drug Information of LUMIGAN
| Product NDC: | 0023-3205 |
| Proprietary Name: | LUMIGAN |
| Non Proprietary Name: | bimatoprost |
| Active Ingredient(s): | .1 mg/mL & nbsp; bimatoprost |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LUMIGAN
| Product NDC: | 0023-3205 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022184 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100910 |
Package Information of LUMIGAN
| Package NDC: | 0023-3205-08 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0023-3205-08) > 7.5 mL in 1 BOTTLE, DROPPER |
NDC Information of LUMIGAN
| NDC Code | 0023-3205-08 |
| Proprietary Name | LUMIGAN |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0023-3205-08) > 7.5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 0023-3205 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bimatoprost |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20100910 |
| Marketing Category Name | NDA |
| Labeler Name | Allergan, Inc. |
| Substance Name | BIMATOPROST |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] |
