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BioGlo
BioGlo - 17238-900-30 - (Fluorescein Sodium)
Drug Information of BioGlo
| Product NDC: | 17238-900 |
| Proprietary Name: | BioGlo |
| Non Proprietary Name: | Fluorescein Sodium |
| Active Ingredient(s): | 1 mg/mg & nbsp; Fluorescein Sodium |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | STRIP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BioGlo
| Product NDC: | 17238-900 |
| Labeler Name: | HUB Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120401 |
Package Information of BioGlo
| Package NDC: | 17238-900-30 |
| Package Description: | 300 PACKET in 1 BOX (17238-900-30) > 1 mg in 1 PACKET (17238-900-99) |
NDC Information of BioGlo
| NDC Code | 17238-900-30 |
| Proprietary Name | BioGlo |
| Package Description | 300 PACKET in 1 BOX (17238-900-30) > 1 mg in 1 PACKET (17238-900-99) |
| Product NDC | 17238-900 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluorescein Sodium |
| Dosage Form Name | STRIP |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20120401 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | HUB Pharmaceuticals, Inc. |
| Substance Name | FLUORESCEIN SODIUM |
| Strength Number | 1 |
| Strength Unit | mg/mg |
| Pharmaceutical Classes | Diagnostic Dye [EPC],Dyes [MoA] |
