NDC 13411-855 Acetamax Pm

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:
13411-855
Proprietary Name:
Acetamax Pm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
Labeler Code:
13411
Start Marketing Date: [9]
08-31-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
22 MM
Score:
1

Product Packages

NDC Code 13411-855-16

Package Description: 16 BLISTER PACK in 1 BOX / 1 TABLET, EFFERVESCENT in 1 BLISTER PACK

NDC Code 13411-855-20

Package Description: 20 BLISTER PACK in 1 BOX / 1 TABLET, EFFERVESCENT in 1 BLISTER PACK

NDC Code 13411-855-24

Package Description: 24 BLISTER PACK in 1 BOX / 1 TABLET, EFFERVESCENT in 1 BLISTER PACK

Product Details

What is NDC 13411-855?

The NDC code 13411-855 is assigned by the FDA to the product Acetamax Pm which is product labeled by Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 13411-855-16 16 blister pack in 1 box / 1 tablet, effervescent in 1 blister pack, 13411-855-20 20 blister pack in 1 box / 1 tablet, effervescent in 1 blister pack, 13411-855-24 24 blister pack in 1 box / 1 tablet, effervescent in 1 blister pack. 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 Acetamax Pm?

Do not take more than directed (see overdose warning)Adults and children 12 years and over:• take 2 tablets fully dissolved in 8oz of water at  bedtime.• do not take more than 2 tablets of this product in 24 hoursChildren under 12 years: do not use

Which are Acetamax Pm UNII Codes?

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

Which are Acetamax Pm 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 Acetamax Pm?

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: 2394042 - acetaminophen 500 MG / diphenhydrAMINE hydrochloride 25 MG Effervescent Oral Tablet
  • RxCUI: 2394042 - acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Effervescent Oral Tablet
  • RxCUI: 2394042 - APAP 500 MG / diphenhydramine hydrochloride 25 MG Effervescent 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".