| Product NDC: | 24208-825 |
| Proprietary Name: | Atropine Sulfate |
| Non Proprietary Name: | Atropine Sulfate |
| Active Ingredient(s): | 10 mg/g & nbsp; Atropine Sulfate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 24208-825 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19900930 |
| Package NDC: | 24208-825-55 |
| Package Description: | 1 TUBE in 1 CARTON (24208-825-55) > 3.5 g in 1 TUBE |
| NDC Code | 24208-825-55 |
| Proprietary Name | Atropine Sulfate |
| Package Description | 1 TUBE in 1 CARTON (24208-825-55) > 3.5 g in 1 TUBE |
| Product NDC | 24208-825 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Atropine Sulfate |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19900930 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | ATROPINE SULFATE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |