Product NDC: | 64272-736 |
Proprietary Name: | AFRICAN SEA-COCONUT |
Non Proprietary Name: | Elm |
Active Ingredient(s): | 65 mg/5mL & nbsp; Elm |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64272-736 |
Labeler Name: | LUEN FOOK MEDICINE SDN. BHD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120601 |
Package NDC: | 64272-736-01 |
Package Description: | 1 BOTTLE, GLASS in 1 BOX (64272-736-01) > 177 mL in 1 BOTTLE, GLASS |
NDC Code | 64272-736-01 |
Proprietary Name | AFRICAN SEA-COCONUT |
Package Description | 1 BOTTLE, GLASS in 1 BOX (64272-736-01) > 177 mL in 1 BOTTLE, GLASS |
Product NDC | 64272-736 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Elm |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20120601 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | LUEN FOOK MEDICINE SDN. BHD. |
Substance Name | ELM |
Strength Number | 65 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |