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ANTIMONIUM TARTARICUM
ANTIMONIUM TARTARICUM - 10191-1842-2 - (Antimony Potassium Tartrate)
Drug Information of ANTIMONIUM TARTARICUM
| Product NDC: | 10191-1842 |
| Proprietary Name: | ANTIMONIUM TARTARICUM |
| Non Proprietary Name: | Antimony Potassium Tartrate |
| Active Ingredient(s): | 9 [hp_C]/1 & nbsp; Antimony Potassium Tartrate |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ANTIMONIUM TARTARICUM
| Product NDC: | 10191-1842 |
| Labeler Name: | Remedy Makers |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20020909 |
Package Information of ANTIMONIUM TARTARICUM
| Package NDC: | 10191-1842-2 |
| Package Description: | 169 PELLET in 1 VIAL, GLASS (10191-1842-2) |
NDC Information of ANTIMONIUM TARTARICUM
| NDC Code | 10191-1842-2 |
| Proprietary Name | ANTIMONIUM TARTARICUM |
| Package Description | 169 PELLET in 1 VIAL, GLASS (10191-1842-2) |
| Product NDC | 10191-1842 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Antimony Potassium Tartrate |
| Dosage Form Name | PELLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20020909 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Remedy Makers |
| Substance Name | ANTIMONY POTASSIUM TARTRATE |
| Strength Number | 9 |
| Strength Unit | [hp_C]/1 |
| Pharmaceutical Classes |
