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Homatropine
Homatropine - 17238-192-05 - (Homatropine Hydrobromide)
Drug Information of Homatropine
| Product NDC: | 17238-192 |
| Proprietary Name: | Homatropine |
| Non Proprietary Name: | Homatropine Hydrobromide |
| Active Ingredient(s): | 50 mg/5mL & nbsp; Homatropine Hydrobromide |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Homatropine
| Product NDC: | 17238-192 |
| Labeler Name: | HUB Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120610 |
Package Information of Homatropine
| Package NDC: | 17238-192-05 |
| Package Description: | 1 BOTTLE in 1 BOX (17238-192-05) > 5 mL in 1 BOTTLE (17238-192-55) |
NDC Information of Homatropine
| NDC Code | 17238-192-05 |
| Proprietary Name | Homatropine |
| Package Description | 1 BOTTLE in 1 BOX (17238-192-05) > 5 mL in 1 BOTTLE (17238-192-55) |
| Product NDC | 17238-192 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Homatropine Hydrobromide |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20120610 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | HUB Pharmaceuticals |
| Substance Name | HOMATROPINE HYDROBROMIDE |
| Strength Number | 50 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Cholinergic Muscarinic Agonist [EPC],Cholinergic Muscarinic Agonists [MoA] |
