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FML
FML - 0023-0316-04 - (fluorometholone)
Drug Information of FML
| Product NDC: | 0023-0316 |
| Proprietary Name: | FML |
| Non Proprietary Name: | fluorometholone |
| Active Ingredient(s): | 1 mg/g & nbsp; fluorometholone |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FML
| Product NDC: | 0023-0316 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017760 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19851209 |
Package Information of FML
| Package NDC: | 0023-0316-04 |
| Package Description: | 1 TUBE in 1 CARTON (0023-0316-04) > 3.5 g in 1 TUBE |
NDC Information of FML
| NDC Code | 0023-0316-04 |
| Proprietary Name | FML |
| Package Description | 1 TUBE in 1 CARTON (0023-0316-04) > 3.5 g in 1 TUBE |
| Product NDC | 0023-0316 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluorometholone |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19851209 |
| Marketing Category Name | NDA |
| Labeler Name | Allergan, Inc. |
| Substance Name | FLUOROMETHOLONE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
