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National Drug Code (NDC)
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VITAMINS A, C, D and FLUORIDE
VITAMINS A, C, D and FLUORIDE - 51862-164-50 - (VITAMINS A, C, D and FLUORIDE)
Drug Information of VITAMINS A, C, D and FLUORIDE
| Product NDC: | 51862-164 |
| Proprietary Name: | VITAMINS A, C, D and FLUORIDE |
| Non Proprietary Name: | VITAMINS A, C, D and FLUORIDE |
| Active Ingredient(s): | 35; 400; .25; 1500 mg/mL; [iU]/mL; mg/mL; [iU]/mL & nbsp; VITAMINS A, C, D and FLUORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VITAMINS A, C, D and FLUORIDE
| Product NDC: | 51862-164 |
| Labeler Name: | Libertas Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110521 |
Package Information of VITAMINS A, C, D and FLUORIDE
| Package NDC: | 51862-164-50 |
| Package Description: | 1 BOTTLE in 1 CARTON (51862-164-50) > 50 mL in 1 BOTTLE |
NDC Information of VITAMINS A, C, D and FLUORIDE
| NDC Code | 51862-164-50 |
| Proprietary Name | VITAMINS A, C, D and FLUORIDE |
| Package Description | 1 BOTTLE in 1 CARTON (51862-164-50) > 50 mL in 1 BOTTLE |
| Product NDC | 51862-164 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | VITAMINS A, C, D and FLUORIDE |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | ORAL |
| Start Marketing Date | 20110521 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Libertas Pharma, Inc. |
| Substance Name | ASCORBIC ACID; CHOLECALCIFEROL; SODIUM FLUORIDE; VITAMIN A PALMITATE |
| Strength Number | 35; 400; .25; 1500 |
| Strength Unit | mg/mL; [iU]/mL; mg/mL; [iU]/mL |
| Pharmaceutical Classes | Vitamin A [Chemical/Ingredient],Vitamin A [EPC] |
