Drugplain

Lomotil .025 mg/1

diphenoxylate hydrochloride and atropine sulfate · TABLET · Pfizer Laboratories Div Pfizer Inc

No Recall History
Plain English

Lomotil is a tablet containing diphenoxylate hydrochloride and atropine sulfate at .025 mg/1, taken oral. Manufactured by Pfizer Laboratories Div Pfizer Inc.

Key Facts

Brand Name
Lomotil
Generic Name
diphenoxylate hydrochloride and atropine sulfate
NDC Code (Product)
0025-0061
Manufacturer
Pfizer Laboratories Div Pfizer Inc
Strength
.025 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
DEA Schedule
Schedule V (Controlled)
Application #
NDA012462
Marketing Start
09/15/1960

Recall History

No Recall History

Frequently Asked Questions

What is Lomotil used for?

Lomotil contains diphenoxylate hydrochloride and atropine sulfate. It is a tablet taken oral. Consult your doctor for specific uses.

Is Lomotil a controlled substance?

Yes, Lomotil is classified as CV under the DEA Controlled Substances Act.

What is the generic name for Lomotil?

The generic name for Lomotil is diphenoxylate hydrochloride and atropine sulfate. There are 11 other brand versions of diphenoxylate hydrochloride and atropine sulfate.

What is the NDC code for Lomotil .025 mg/1?

The NDC (National Drug Code) for Lomotil .025 mg/1 is 0025-0061, listed by Pfizer Laboratories Div Pfizer Inc.