Search by Drug Name or NDC
NDC 59088-0695-54 Davimet 10; 24; 10; 4.5; 1667; 13.5; 1.05; 1.2; 36; 1.05; 750 mg/1; mg/1; ug/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1 Details
Davimet 10; 24; 10; 4.5; 1667; 13.5; 1.05; 1.2; 36; 1.05; 750 mg/1; mg/1; ug/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1
Davimet is a ORAL TABLET, CHEWABLE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PureTek Corporation. The primary component is .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CHOLECALCIFEROL; CYANOCOBALAMIN; FOLIC ACID; NIACIN; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONONITRATE; VITAMIN A.
Product Information
| NDC | 59088-0695 |
|---|---|
| Product ID | 59088-695_0c67d713-8906-2a32-e063-6394a90a8510 |
| Associated GPIs | |
| GCN Sequence Number | 084000 |
| GCN Sequence Number Description | multivitamin no.58/folic acid TAB CHEW 1000 MCG ORAL |
| HIC3 | C6Z |
| HIC3 Description | MULTIVITAMIN PREPARATIONS |
| GCN | 53096 |
| HICL Sequence Number | 048428 |
| HICL Sequence Number Description | MULTIVITAMIN COMBINATION NO.58/FOLIC ACID |
| Brand/Generic | Brand |
| Proprietary Name | Davimet |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Multivitamin |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, CHEWABLE |
| Route | ORAL |
| Active Ingredient Strength | 10; 24; 10; 4.5; 1667; 13.5; 1.05; 1.2; 36; 1.05; 750 |
| Active Ingredient Units | mg/1; mg/1; ug/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1 |
| Substance Name | .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CHOLECALCIFEROL; CYANOCOBALAMIN; FOLIC ACID; NIACIN; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONONITRATE; VITAMIN A |
| Labeler Name | PureTek Corporation |
| Pharmaceutical Class | Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Ascorbic Acid [CS], Nicotinic Acid [EPC], Nicotinic Acids [CS], Vitamin A [CS], Vitamin A [EPC], Vitamin B 12 [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B12 [EPC], Vitamin B6 Analog [EPC |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 59088-0695-54 (59088069554)
| NDC Package Code | 59088-695-54 |
|---|---|
| Billing NDC | 59088069554 |
| Package | 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (59088-695-54) |
| Marketing Start Date | 2022-09-19 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |