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Fresh Morning Bifidus
Fresh Morning Bifidus - 51220-1001-1 - (lactobacillus)
Drug Information of Fresh Morning Bifidus
| Product NDC: | 51220-1001 |
| Proprietary Name: | Fresh Morning Bifidus |
| Non Proprietary Name: | lactobacillus |
| Active Ingredient(s): | .0316 mg/mg & nbsp; lactobacillus |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fresh Morning Bifidus
| Product NDC: | 51220-1001 |
| Labeler Name: | Saimdang Cosmetics Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100821 |
Package Information of Fresh Morning Bifidus
| Package NDC: | 51220-1001-1 |
| Package Description: | 2000 mg in 1 POUCH (51220-1001-1) |
NDC Information of Fresh Morning Bifidus
| NDC Code | 51220-1001-1 |
| Proprietary Name | Fresh Morning Bifidus |
| Package Description | 2000 mg in 1 POUCH (51220-1001-1) |
| Product NDC | 51220-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | lactobacillus |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 20100821 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Saimdang Cosmetics Co., Ltd |
| Substance Name | LACTIC ACID |
| Strength Number | .0316 |
| Strength Unit | mg/mg |
| Pharmaceutical Classes |
