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  4. NDC Product Code: 70859-061 Mpm Pak

NDC 70859-061 Mpm Pak

Kit - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 70859-061?
  5. Mpm Pak Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

NDC Product Code:
70859-061
Proprietary Name:
Mpm Pak
Non-Proprietary Name: [1]
Mpm Pak
NDC Directory Status:
Human Prescription Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Nucare Pharmaceuticals,inc.
Labeler Code:
70859
Product Label ID:
fe1e8a02-bbef-ab0f-e053-6394a90aa466
FDA Application Number: [6]
ANDA091178
Marketing Category: [8]
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date: [9]
06-14-2023
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
WHITE (C48325 - WHITE TO OFF-WHITE)
YELLOW (C48330)
Shape:
HEXAGON (6 SIDED) (C48343)
CAPSULE (C48336)
ROUND (C48348)
Size(s):
9 MM
19 MM
11 MM
7 MM
Imprint(s):
G;5008
I8
S
7;E
Score:
2
1
Flavor(s):
GUARANA (C73393)
STRAWBERRY (C73417)

Code Structure Chart

Product Details

What is NDC 70859-061?

The NDC code 70859-061 is assigned by the FDA to the product Mpm Pak which is a human prescription drug product labeled by Nucare Pharmaceuticals,inc.. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 70859-061-01 1 kit in 1 kit * 12 tablet in 1 bottle (68071-2903-7) * 1 tablet in 1 blister pack (43393-001-01) * 1 blister pack in 1 carton (68071-2865-1) / 10 tablet, orally disintegrating in 1 blister pack * 4 tablet in 1 bottle (43393-020-04). 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 Mpm Pak?

Mifepristone tablets, 200 mg is indicated, in a regimen with misoprostol, for the medical termination of intrauterine pregnancy through 70 days gestation. Ondansetron orally disintegrating tablets are indicated for the prevention of nausea and vomiting associated with:highly emetogenic cancer chemotherapy, including cisplatin greater than or equal to 50 mg/m 2initial and repeat courses of moderately emetogenic cancer chemotherapyradiotherapy in patients receiving either total body irradiation, single high-dose fraction to the abdomen, or daily fractions to the abdomenOndansetron orally disintegrating tablets also indicated for the prevention of postoperative nausea and/or vomiting.

Which are Mpm Pak UNII Codes?

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

Which are Mpm Pak 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 Mpm Pak?

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:

* Please review the disclaimer below.

Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

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

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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".