Drugplain

Buprenorphine Sublingual 2 mg/1

Buprenorphine Sublingual · TABLET · Direct_rx

No Recall History
Plain English

Buprenorphine Sublingual is a tablet containing buprenorphine sublingual at 2 mg/1, taken sublingual. Manufactured by Direct_rx.

Key Facts

Brand Name
Buprenorphine Sublingual
Generic Name
Buprenorphine Sublingual
NDC Code (Product)
72189-579
Manufacturer
Direct_rx
Strength
2 mg/1
Dosage Form
TABLET
Route
SUBLINGUAL
Marketing Status
DEA Schedule
Schedule III (Controlled)
Application #
ANDA201760
Marketing Start
09/13/2024

Recall History

No Recall History

Frequently Asked Questions

What is Buprenorphine Sublingual used for?

Buprenorphine Sublingual contains Buprenorphine Sublingual. It is a tablet taken sublingual. Consult your doctor for specific uses.

Is Buprenorphine Sublingual a controlled substance?

Yes, Buprenorphine Sublingual is classified as CIII under the DEA Controlled Substances Act.

What is the generic name for Buprenorphine Sublingual?

The generic name for Buprenorphine Sublingual is Buprenorphine Sublingual. There are 2 other brand versions of Buprenorphine Sublingual.

What is the NDC code for Buprenorphine Sublingual 2 mg/1?

The NDC (National Drug Code) for Buprenorphine Sublingual 2 mg/1 is 72189-579, listed by Direct_rx.

Product NDC

72189-579

Package NDC

72189-579-60

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

Data from openFDA · Public domain (CC0 1.0)