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371 (Oxycodone Hydrochloride 20 mg)

Pill with imprint 371 is Gray, Round and has been identified as Oxycodone Hydrochloride 20 mg. It is supplied by Sun Pharmaceutical Industries Inc..

Oxycodone is used in the treatment of chronic pain; pain and belongs to the drug class narcotic analgesics. FDA has not classified the drug for risk during pregnancy. Oxycodone 20 mg is classified as a Schedule 2 controlled substance under the Controlled Substance Act (CSA).

Images for 371

Oxycodone Hydrochloride

Imprint
371
Strength
20 mg
Color
Gray
Size
6.00 mm
Shape
Round
Availability
Prescription only
Drug Class
Narcotic analgesics
Pregnancy Category
N - Not classified
CSA Schedule
2 - High potential for abuse
Labeler / Supplier
Sun Pharmaceutical Industries Inc.
National Drug Code (NDC)
57664-0371
Inactive Ingredients
lactose anhydrous, silicon dioxide, magnesium stearate, microcrystalline cellulose, corn starch, sodium starch glycolate type A potato, FD&C Blue No. 1, FD&C Blue No. 2, FD&C Yellow No. 6, FD&C Red No. 40

Note: Inactive ingredients may vary.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.