Product NDC: | 17478-214 |
Proprietary Name: | Atropine Sulfate |
Non Proprietary Name: | Atropine Sulfate |
Active Ingredient(s): | 10 mg/mL & nbsp; Atropine Sulfate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17478-214 |
Labeler Name: | Akorn, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19950601 |
Package NDC: | 17478-214-12 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (17478-214-12) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 17478-214-12 |
Proprietary Name | Atropine Sulfate |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (17478-214-12) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 17478-214 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Atropine Sulfate |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 19950601 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Akorn, Inc. |
Substance Name | ATROPINE SULFATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |