| Product NDC: | 10191-1225 |
| Proprietary Name: | APOMORPHINUM MURIATICUM |
| Non Proprietary Name: | APOMORPHINE HYDROCHLORIDE |
| Active Ingredient(s): | 3 [hp_X]/1 & nbsp; APOMORPHINE HYDROCHLORIDE |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10191-1225 |
| Labeler Name: | Remedy Makers |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20020318 |
| Package NDC: | 10191-1225-2 |
| Package Description: | 153 PELLET in 1 VIAL, GLASS (10191-1225-2) |
| NDC Code | 10191-1225-2 |
| Proprietary Name | APOMORPHINUM MURIATICUM |
| Package Description | 153 PELLET in 1 VIAL, GLASS (10191-1225-2) |
| Product NDC | 10191-1225 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | APOMORPHINE HYDROCHLORIDE |
| Dosage Form Name | PELLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20020318 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Remedy Makers |
| Substance Name | APOMORPHINE HYDROCHLORIDE |
| Strength Number | 3 |
| Strength Unit | [hp_X]/1 |
| Pharmaceutical Classes | Dopamine Agonists [MoA],Dopaminergic Agonist [EPC] |