Drugplain

Lactistat 12 [hp_X]/mL

Arsenicum Album, Calcarea Carbonica, Cocculus Indicus, Graphites, Hydrofluoricum Acidum, Lachesis Mutus, Lacticum Acidum, Rhus Tox, Ruta Graveolens, Sarcolacticum Acidum, Saccharum Officinale · LIQUID · Energique, Inc.

No Recall History
Plain English

Lactistat is a liquid containing arsenicum album, calcarea carbonica, cocculus indicus, graphites, hydrofluoricum acidum, lachesis mutus, lacticum acidum, rhus tox, ruta graveolens, sarcolacticum acidum, saccharum officinale at 12 [hp_X]/mL, taken oral. Manufactured by Energique, Inc..

Key Facts

Brand Name
Lactistat
Generic Name
Arsenicum Album, Calcarea Carbonica, Cocculus Indicus, Graphites, Hydrofluoricum Acidum, Lachesis Mutus, Lacticum Acidum, Rhus Tox, Ruta Graveolens, Sarcolacticum Acidum, Saccharum Officinale
NDC Code (Product)
44911-0336
Manufacturer
Energique, Inc.
Strength
12 [hp_X]/mL
Dosage Form
LIQUID
Route
ORAL
Marketing Status
Marketing Start
03/30/2016

Recall History

No Recall History

Frequently Asked Questions

What is Lactistat used for?

Lactistat contains Arsenicum Album, Calcarea Carbonica, Cocculus Indicus, Graphites, Hydrofluoricum Acidum, Lachesis Mutus, Lacticum Acidum, Rhus Tox, Ruta Graveolens, Sarcolacticum Acidum, Saccharum Officinale. It is a liquid taken oral. Consult your doctor for specific uses.

Is Lactistat a controlled substance?

Lactistat is not classified as a controlled substance by the DEA.

What is the generic name for Lactistat?

The generic name for Lactistat is Arsenicum Album, Calcarea Carbonica, Cocculus Indicus, Graphites, Hydrofluoricum Acidum, Lachesis Mutus, Lacticum Acidum, Rhus Tox, Ruta Graveolens, Sarcolacticum Acidum, Saccharum Officinale. There are no other listed brand versions of Arsenicum Album, Calcarea Carbonica, Cocculus Indicus, Graphites, Hydrofluoricum Acidum, Lachesis Mutus, Lacticum Acidum, Rhus Tox, Ruta Graveolens, Sarcolacticum Acidum, Saccharum Officinale.

What is the NDC code for Lactistat 12 [hp_X]/mL?

The NDC (National Drug Code) for Lactistat 12 [hp_X]/mL is 44911-0336, listed by Energique, Inc..

Product NDC

44911-0336

Package NDC

44911-0336-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)