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  4. NDC Product Code: 16638-118 Citramon

NDC 16638-118 Citramon

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 16638-118?
  5. Citramon Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
16638-118
Proprietary Name:
Citramon
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Borisovskiy Zavod Medicinskikh Preparatov Jsc
Labeler Code:
16638
Product Label ID:
4ecaba53-e879-405c-826a-5659686239b5
Start Marketing Date: [9]
06-26-1996
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - LIGHT BROWN WITH WHITE INCLUSIONS)
Shape:
ROUND (C48348)
Size(s):
12 MM
Score:
2
Flavor(s):
COFFEE (C73380 - COFFEE FLAVOR)

Code Structure Chart

Product Details

What is NDC 16638-118?

The NDC code 16638-118 is assigned by the FDA to the product Citramon which is product labeled by Borisovskiy Zavod Medicinskikh Preparatov Jsc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 16638-118-13 3300 mg in 1 package . 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 Citramon?

Adults and children over 15 years take 1 tablet 2 - 3 times a day. The interval between the drug intakes should be at least 6 - 8 hours. Maximum single dose is 2 tablets, maximum daily dose is 4 tablets.

Which are Citramon UNII Codes?

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

Which are Citramon Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Citramon?

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:
  • RxCUI: 1673788 - acetaminophen 200 MG / aspirin 220 MG / caffeine 27 MG Oral Tablet
  • RxCUI: 1673788 - APAP 200 MG / ASA 220 MG / Caffeine 27 MG Oral Tablet

* Please review the disclaimer below.

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".