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Sucrose
Sucrose - 48951-9999-2 - (SUCROSE)
Drug Information of Sucrose
| Product NDC: | 48951-9999 |
| Proprietary Name: | Sucrose |
| Non Proprietary Name: | SUCROSE |
| Active Ingredient(s): | 1 [hp_X]/1 & nbsp; SUCROSE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sucrose
| Product NDC: | 48951-9999 |
| Labeler Name: | Uriel Pharmacy Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20100201 |
Package Information of Sucrose
| Package NDC: | 48951-9999-2 |
| Package Description: | 1350 PELLET in 1 BOTTLE, GLASS (48951-9999-2) |
NDC Information of Sucrose
| NDC Code | 48951-9999-2 |
| Proprietary Name | Sucrose |
| Package Description | 1350 PELLET in 1 BOTTLE, GLASS (48951-9999-2) |
| Product NDC | 48951-9999 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SUCROSE |
| Dosage Form Name | PELLET |
| Route Name | ORAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Uriel Pharmacy Inc |
| Substance Name | SUCROSE |
| Strength Number | 1 |
| Strength Unit | [hp_X]/1 |
| Pharmaceutical Classes |
