Anatra 200 [hp_C]/1

Anas Barbariae · TABLET · Anatra LLC

No Recall History

Plain English

Anatra is an over-the-counter oral tablet containing Anas barbariae that is commonly used to help relieve symptoms of colds and flu. The product is available without a prescription for patients seeking natural symptom relief.

Key Facts

Brand Name: Anatra
Generic Name: Anas Barbariae
NDC Code (Product): 83641-001
Manufacturer: Anatra LLC
Strength: 200 [hp_C]/1
Dosage Form: TABLET
Route: ORAL
Marketing Status
Marketing Start: 09/01/2023

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses Temporarily relieves cold & flu-like symptoms such as: Body aches Headache Fever Chills Fatigue

Dosage & Administration

Directions ANATRA may be taken regularly as a preventative. Adults and children 2 years of age and older: Dissolve entire tablet in mouth every 6 hours, up to 3 times a day. Children under two years of age: Ask a Doctor.

Warnings

Warnings Ask a Doctor before use in children under 2 years of age. Stop use and ask a Doctor if symptoms persist for more than 3 days or worsen. If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children.

Frequently Asked Questions

What is Anatra used for?

Is Anatra a controlled substance?

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

What is the generic name for Anatra?

The generic name for Anatra is Anas Barbariae. There are 11 other brand versions of Anas Barbariae.

What is the NDC code for Anatra 200 [hp_C]/1?

The NDC (National Drug Code) for Anatra 200 [hp_C]/1 is 83641-001, listed by Anatra LLC.

Product NDC

83641-001

Package NDC

83641-001-01

Other Anas Brands

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

Data from openFDA · Public domain (CC0 1.0)