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  4. NDC Product Code: 70898-115 Neonatal Plus Vitamin

NDC 70898-115 Neonatal Plus Vitamin

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 70898-115?
  5. Neonatal Plus Vitamin Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70898-115
Proprietary Name:
Neonatal Plus Vitamin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Neomed Pharmaceutical
Labeler Code:
70898
Product Label ID:
d6f0af28-1e4a-4b06-9ff5-fc15f3f13ea9
Start Marketing Date: [9]
07-31-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - BEIGE/PEACH)
Shape:
CAPSULE (C48336)
Size(s):
5 MM
Score:
1

Code Structure Chart

Product Details

What is NDC 70898-115?

The NDC code 70898-115 is assigned by the FDA to the product Neonatal Plus Vitamin which is product labeled by Neomed Pharmaceutical. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70898-115-01 1 bottle in 1 package / 100 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 are the uses for Neonatal Plus Vitamin?

NEONATAL PLUS TABLET  Rx is a multi-vitamin/mineral prescription drug indicated for use in improving the nutritional status of women prior to conception, throughout pregnancy, and in the postnatal period for both lactating and nonlactating mothers.

Which are Neonatal Plus Vitamin UNII Codes?

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

Which are Neonatal Plus Vitamin 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:

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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".