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Letomint
Letomint - 76255-2001-1 - (clove)
Drug Information of Letomint
| Product NDC: | 76255-2001 |
| Proprietary Name: | Letomint |
| Non Proprietary Name: | clove |
| Active Ingredient(s): | 18 mg/1 & nbsp; clove |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Letomint
| Product NDC: | 76255-2001 |
| Labeler Name: | H&C 21 America Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110618 |
Package Information of Letomint
| Package NDC: | 76255-2001-1 |
| Package Description: | 18 TABLET in 1 BOX (76255-2001-1) |
NDC Information of Letomint
| NDC Code | 76255-2001-1 |
| Proprietary Name | Letomint |
| Package Description | 18 TABLET in 1 BOX (76255-2001-1) |
| Product NDC | 76255-2001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | clove |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110618 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | H&C 21 America Inc |
| Substance Name | CLOVE |
| Strength Number | 18 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
