NDC 63187-949 Promethazine Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63187-949
Proprietary Name:
Promethazine Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Proficient Rx Lp
Labeler Code:
63187
Start Marketing Date: [9]
03-03-2011
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 63187-949-10

Package Description: 10 TABLET in 1 BOTTLE

NDC Code 63187-949-12

Package Description: 12 TABLET in 1 BOTTLE

NDC Code 63187-949-15

Package Description: 15 TABLET in 1 BOTTLE

NDC Code 63187-949-20

Package Description: 20 TABLET in 1 BOTTLE

NDC Code 63187-949-30

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 63187-949-60

Package Description: 60 TABLET in 1 BOTTLE

NDC Code 63187-949-90

Package Description: 90 TABLET in 1 BOTTLE

Product Details

What is NDC 63187-949?

The NDC code 63187-949 is assigned by the FDA to the product Promethazine Hydrochloride which is product labeled by Proficient Rx Lp. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 63187-949-10 10 tablet in 1 bottle , 63187-949-12 12 tablet in 1 bottle , 63187-949-15 15 tablet in 1 bottle , 63187-949-20 20 tablet in 1 bottle , 63187-949-30 30 tablet in 1 bottle , 63187-949-60 60 tablet in 1 bottle , 63187-949-90 90 tablet in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What is the NDC to RxNorm Crosswalk for Promethazine Hydrochloride?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Patient Education

Promethazine


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.
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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".