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  4. NDC Product Code: 33358-903 Megestrol Acetate

NDC 33358-903 Megestrol Acetate

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 33358-903?
  5. Megestrol Acetate Uses
  6. Active Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
33358-903
Proprietary Name:
Megestrol Acetate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rxchange Co
Labeler Code:
33358
Product Label ID:
3c02f4fb-2d1f-3529-e054-00144ff88e88
Start Marketing Date: [9]
07-25-2001
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - MILKY WHITE)
Flavor(s):
LIME (C73398)
LEMON (C73396)

Code Structure Chart

Product Details

What is NDC 33358-903?

The NDC code 33358-903 is assigned by the FDA to the product Megestrol Acetate which is product labeled by Rxchange Co. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 33358-903-05 5 ml in 1 cup, unit-dose , 33358-903-10 10 ml in 1 cup, unit-dose , 33358-903-20 20 ml in 1 cup, unit-dose . 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 are the uses for Megestrol Acetate?

Megestrol is used to treat loss of appetite and weight loss in people with AIDS. Improving your appetite and gaining weight may help you feel better and be more active. Megestrol is similar to a natural substance made by the body called progesterone.

Which are Megestrol Acetate UNII Codes?

The UNII codes for the active ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Megestrol Acetate?

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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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".