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Phospholine Iodide
Phospholine Iodide - 0046-1065-05 - (echothiophate iodide)
Drug Information of Phospholine Iodide
| Product NDC: | 0046-1065 |
| Proprietary Name: | Phospholine Iodide |
| Non Proprietary Name: | echothiophate iodide |
| Active Ingredient(s): | & nbsp; echothiophate iodide |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phospholine Iodide
| Product NDC: | 0046-1065 |
| Labeler Name: | Wyeth Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011963 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19591204 |
Package Information of Phospholine Iodide
| Package NDC: | 0046-1065-05 |
| Package Description: | 1 KIT in 1 KIT (0046-1065-05) * 6.25 mL in 1 BOTTLE (0046-1465-05) * 5 mL in 1 BOTTLE (0046-1162-05) |
NDC Information of Phospholine Iodide
| NDC Code | 0046-1065-05 |
| Proprietary Name | Phospholine Iodide |
| Package Description | 1 KIT in 1 KIT (0046-1065-05) * 6.25 mL in 1 BOTTLE (0046-1465-05) * 5 mL in 1 BOTTLE (0046-1162-05) |
| Product NDC | 0046-1065 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | echothiophate iodide |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19591204 |
| Marketing Category Name | NDA |
| Labeler Name | Wyeth Pharmaceuticals Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
