Drugplain

SEPIA 200ck 200 [kp_C]/1

SEPIA · PELLET · SEVENE USA

No Recall History
Plain English

SEPIA 200ck is a pellet containing sepia at 200 [kp_C]/1, taken sublingual. Manufactured by SEVENE USA.

Key Facts

Brand Name
SEPIA 200ck
Generic Name
SEPIA
NDC Code (Product)
76472-3033
Manufacturer
SEVENE USA
Strength
200 [kp_C]/1
Dosage Form
PELLET
Route
SUBLINGUAL
Marketing Status
Marketing Start
11/23/2011

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

fatigue2 reports
bladder transitional cell carcinoma1 reports
chills1 reports
depressed level of consciousness1 reports
diarrhoea1 reports
endometrial cancer stage i1 reports
exostosis1 reports
fall1 reports
feeling abnormal1 reports
frequent bowel movements1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

USE Condition listed above or as directed by a physician.

Dosage & Administration

DIRECTIONS (adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

Warnings

WARNINGS Stop use and ask a physician if symptoms persist for more than 3 days or worsen.

Frequently Asked Questions

What is SEPIA 200ck used for?

SEPIA 200ck contains SEPIA. It is a pellet taken sublingual. Consult your doctor for specific uses.

Is SEPIA 200ck a controlled substance?

SEPIA 200ck is not classified as a controlled substance by the DEA.

What is the generic name for SEPIA 200ck?

The generic name for SEPIA 200ck is SEPIA. There are 12 other brand versions of SEPIA.

What is the NDC code for SEPIA 200ck 200 [kp_C]/1?

The NDC (National Drug Code) for SEPIA 200ck 200 [kp_C]/1 is 76472-3033, listed by SEVENE USA.

Product NDC

76472-3033

Package NDC

76472-3033-1

Other Sepia 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)