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Miochol E
Miochol E - 0078-0474-61 - (acetylcholine chloride)
Drug Information of Miochol E
| Product NDC: | 0078-0474 |
| Proprietary Name: | Miochol E |
| Non Proprietary Name: | acetylcholine chloride |
| Active Ingredient(s): | & nbsp; acetylcholine chloride |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Miochol E
| Product NDC: | 0078-0474 |
| Labeler Name: | Novartis Pharmaceuticals Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020213 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19930922 |
Package Information of Miochol E
| Package NDC: | 0078-0474-61 |
| Package Description: | 1 KIT in 1 BLISTER PACK (0078-0474-61) * 2 mL in 1 VIAL * 2 mL in 1 AMPULE |
NDC Information of Miochol E
| NDC Code | 0078-0474-61 |
| Proprietary Name | Miochol E |
| Package Description | 1 KIT in 1 BLISTER PACK (0078-0474-61) * 2 mL in 1 VIAL * 2 mL in 1 AMPULE |
| Product NDC | 0078-0474 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acetylcholine chloride |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19930922 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Pharmaceuticals Corporation |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
