Product NDC: | 44911-0025 |
Proprietary Name: | Acetylcholine Chloride Phenolic |
Non Proprietary Name: | Acetylcholine chloride, |
Active Ingredient(s): | 6 [hp_X]/mL & nbsp; Acetylcholine chloride, |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 44911-0025 |
Labeler Name: | Energique, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20121108 |
Package NDC: | 44911-0025-1 |
Package Description: | 30 mL in 1 BOTTLE, DROPPER (44911-0025-1) |
NDC Code | 44911-0025-1 |
Proprietary Name | Acetylcholine Chloride Phenolic |
Package Description | 30 mL in 1 BOTTLE, DROPPER (44911-0025-1) |
Product NDC | 44911-0025 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetylcholine chloride, |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20121108 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Energique, Inc. |
Substance Name | ACETYLCHOLINE CHLORIDE |
Strength Number | 6 |
Strength Unit | [hp_X]/mL |
Pharmaceutical Classes |