Home
>
National Drug Code (NDC)
>
Prostigmin
Prostigmin - 0187-3100-10 - (neostigmine bromide)
Drug Information of Prostigmin
| Product NDC: | 0187-3100 |
| Proprietary Name: | Prostigmin |
| Non Proprietary Name: | neostigmine bromide |
| Active Ingredient(s): | 15 mg/1 & nbsp; neostigmine bromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prostigmin
| Product NDC: | 0187-3100 |
| Labeler Name: | Valeant Pharmaceuticals North America LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20040601 |
Package Information of Prostigmin
| Package NDC: | 0187-3100-10 |
| Package Description: | 100 TABLET in 1 BOTTLE (0187-3100-10) |
NDC Information of Prostigmin
| NDC Code | 0187-3100-10 |
| Proprietary Name | Prostigmin |
| Package Description | 100 TABLET in 1 BOTTLE (0187-3100-10) |
| Product NDC | 0187-3100 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | neostigmine bromide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040601 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Valeant Pharmaceuticals North America LLC |
| Substance Name | NEOSTIGMINE BROMIDE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
