Drugplain

Butalbital and Acetaminophen 300 mg/1

Butalbital and Acetaminophen tablets · TABLET · Oceanside Pharmaceuticals

No Recall History
Plain English

Butalbital and Acetaminophen is a tablet containing butalbital and acetaminophen tablets at 300 mg/1, taken oral. Manufactured by Oceanside Pharmaceuticals.

Key Facts

Brand Name
Butalbital and Acetaminophen
Generic Name
Butalbital and Acetaminophen tablets
NDC Code (Product)
68682-306
Manufacturer
Oceanside Pharmaceuticals
Strength
300 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
DEA Schedule
Schedule III (Controlled)
Application #
ANDA090956
Drug Class
Barbiturate [EPC]
Marketing Start
06/19/2017

Recall History

No Recall History

Frequently Asked Questions

What is Butalbital and Acetaminophen used for?

Butalbital and Acetaminophen contains Butalbital and Acetaminophen tablets. It is a tablet taken oral. Consult your doctor for specific uses.

Is Butalbital and Acetaminophen a controlled substance?

Yes, Butalbital and Acetaminophen is classified as CIII under the DEA Controlled Substances Act.

What is the generic name for Butalbital and Acetaminophen?

The generic name for Butalbital and Acetaminophen is Butalbital and Acetaminophen tablets. There are no other listed brand versions of Butalbital and Acetaminophen tablets.

What is the NDC code for Butalbital and Acetaminophen 300 mg/1?

The NDC (National Drug Code) for Butalbital and Acetaminophen 300 mg/1 is 68682-306, listed by Oceanside Pharmaceuticals.

Product NDC

68682-306

Package NDC

68682-306-01

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

Data from openFDA · Public domain (CC0 1.0)