Drugplain

Ampigrin Ultra Forte Night 325 mg/1

Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate · CAPSULE, LIQUID FILLED · OPMX LLC

No Recall HistoryCurrently in Shortage
Plain English

Ampigrin Ultra Forte Night is a capsule, liquid filled containing acetaminophen, dextromethorphan hydrobromide, doxylamine succinate at 325 mg/1, taken oral. Manufactured by OPMX LLC.

Key Facts

Brand Name
Ampigrin Ultra Forte Night
Generic Name
Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate
NDC Code (Product)
69729-003
Manufacturer
OPMX LLC
Strength
325 mg/1
Dosage Form
CAPSULE, LIQUID FILLED
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
06/10/2022

Recall History

No Recall History

Frequently Asked Questions

What is Ampigrin Ultra Forte Night used for?

Ampigrin Ultra Forte Night contains Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate. It is a capsule, liquid filled taken oral. Consult your doctor for specific uses.

Is Ampigrin Ultra Forte Night a controlled substance?

Ampigrin Ultra Forte Night is not classified as a controlled substance by the DEA.

What is the generic name for Ampigrin Ultra Forte Night?

The generic name for Ampigrin Ultra Forte Night is Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate. There are 12 other brand versions of Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate.

What is the NDC code for Ampigrin Ultra Forte Night 325 mg/1?

The NDC (National Drug Code) for Ampigrin Ultra Forte Night 325 mg/1 is 69729-003, listed by OPMX LLC.