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NDC 59088-0156-54 Menatrol 220; 600; 1000; 100; 1.5; 4 mg/1; [iU]/1; ug/1; mg/1; mg/1; mg/1 Details
Menatrol 220; 600; 1000; 100; 1.5; 4 mg/1; [iU]/1; ug/1; mg/1; mg/1; mg/1
Menatrol is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PureTek Corporation. The primary component is CALCIUM CARBONATE; CHOLECALCIFEROL; LEVOMEFOLATE CALCIUM; MAGNESIUM OXIDE; PYRIDOXINE HYDROCHLORIDE; RHUBARB.
Product Information
NDC | 59088-0156 |
---|---|
Product ID | 59088-156_0a100e7d-3a8e-2d8b-e063-6394a90a3203 |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Menatrol |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Folate, Multivitamin |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | CAPSULE |
Route | ORAL |
Active Ingredient Strength | 220; 600; 1000; 100; 1.5; 4 |
Active Ingredient Units | mg/1; [iU]/1; ug/1; mg/1; mg/1; mg/1 |
Substance Name | CALCIUM CARBONATE; CHOLECALCIFEROL; LEVOMEFOLATE CALCIUM; MAGNESIUM OXIDE; PYRIDOXINE HYDROCHLORIDE; RHUBARB |
Labeler Name | PureTek Corporation |
Pharmaceutical Class | Allergens [CS], Analogs/Derivatives [Chemical/Ingredient], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Folate Analog [EPC], Folic Acid [CS], Inc |
DEA Schedule | n/a |
Marketing Category | UNAPPROVED DRUG OTHER |
Application Number | n/a |
Listing Certified Through | 2024-12-31 |
Package
NDC 59088-0156-54 (59088015654)
NDC Package Code | 59088-156-54 |
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Billing NDC | 59088015654 |
Package | 30 CAPSULE in 1 BOTTLE, PLASTIC (59088-156-54) |
Marketing Start Date | 2023-12-18 |
NDC Exclude Flag | N |
Pricing Information | N/A |