| Product NDC: | 0998-0311 |
| Proprietary Name: | Isopto Homatropine |
| Non Proprietary Name: | homatropine hydrobromide |
| Active Ingredient(s): | 20 mg/mL & nbsp; homatropine hydrobromide |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0998-0311 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19810619 |
| Package NDC: | 0998-0311-05 |
| Package Description: | 5 mL in 1 BOTTLE, DROPPER (0998-0311-05) |
| NDC Code | 0998-0311-05 |
| Proprietary Name | Isopto Homatropine |
| Package Description | 5 mL in 1 BOTTLE, DROPPER (0998-0311-05) |
| Product NDC | 0998-0311 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | homatropine hydrobromide |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19810619 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | HOMATROPINE HYDROBROMIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Cholinergic Muscarinic Agonist [EPC],Cholinergic Muscarinic Agonists [MoA] |