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OPIUM
OPIUM - 10191-1093-2 - (RAW OPIUM GUM)
Drug Information of OPIUM
| Product NDC: | 10191-1093 |
| Proprietary Name: | OPIUM |
| Non Proprietary Name: | RAW OPIUM GUM |
| Active Ingredient(s): | 30 [hp_C]/1 & nbsp; RAW OPIUM GUM |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OPIUM
| Product NDC: | 10191-1093 |
| Labeler Name: | Remedy Makers |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20011121 |
Package Information of OPIUM
| Package NDC: | 10191-1093-2 |
| Package Description: | 137 PELLET in 1 VIAL, GLASS (10191-1093-2) |
NDC Information of OPIUM
| NDC Code | 10191-1093-2 |
| Proprietary Name | OPIUM |
| Package Description | 137 PELLET in 1 VIAL, GLASS (10191-1093-2) |
| Product NDC | 10191-1093 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | RAW OPIUM GUM |
| Dosage Form Name | PELLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20011121 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Remedy Makers |
| Substance Name | OPIUM |
| Strength Number | 30 |
| Strength Unit | [hp_C]/1 |
| Pharmaceutical Classes |
