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NDC 51655-0140-53 Promethazine Hydrochloride 25 mg/1 Details

Promethazine Hydrochloride 25 mg/1

Promethazine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is PROMETHAZINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Promethazine is used to relieve the symptoms of allergic reactions such as allergic rhinitis (runny nose and watery eyes caused by allergy to pollen, mold or dust), allergic conjunctivitis (red, watery eyes caused by allergies), allergic skin reactions, and allergic reactions to blood or plasma products. Promethazine is used with other medications to treat anaphylaxis (sudden, severe allergic reactions) and the symptoms of the common cold such as sneezing, cough, and runny nose. Promethazine is also used to relax and sedate patients before and after surgery, during labor, and at other times. Promethazine is also used to prevent and control nausea and vomiting that may occur after surgery, and with other medications to help relieve pain after surgery. Promethazine is also used to prevent and treat motion sickness. Promethazine helps control symptoms, but will not treat the cause of the symptoms or speed recovery. Promethazine is in a class of medications called phenothiazines. It works by blocking the action of a certain natural substance in the body.

Related Packages: 51655-0140-53
Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Promethazine

Product Information

NDC	51655-0140
Product ID	51655-140_f6ca1097-1c76-c682-e053-6294a90a2bd6
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Promethazine Hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Promethazine Hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	25
Active Ingredient Units	mg/1
Substance Name	PROMETHAZINE HYDROCHLORIDE
Labeler Name	Northwind Pharmaceuticals, LLC
Pharmaceutical Class	Phenothiazine [EPC], Phenothiazines [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA083426
Listing Certified Through	2024-12-31

Package

NDC 51655-0140-53 (51655014053)

Pricing Information	N/A
NDC Package Code	51655-140-53
Billing NDC	51655014053
Package	10 TABLET in 1 BOTTLE, PLASTIC (51655-140-53)
Marketing Start Date	2023-02-03
NDC Exclude Flag	N