NDC 50090-0617 Pnv Prenatal Plus Multivitamin

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:
50090-0617
Proprietary Name:
Pnv Prenatal Plus Multivitamin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
A-s Medication Solutions
Labeler Code:
50090
Start Marketing Date: [9]
04-01-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - OFF-WHITE SPECKLED)
Shape:
OVAL (C48345)
Size(s):
19 MM
Imprint(s):
SCI7
Score:
1

Product Packages

NDC Code 50090-0617-0

Package Description: 100 TABLET in 1 BOTTLE, PLASTIC

NDC Code 50090-0617-1

Package Description: 30 TABLET in 1 BOTTLE

Product Details

What is NDC 50090-0617?

The NDC code 50090-0617 is assigned by the FDA to the product Pnv Prenatal Plus Multivitamin which is product labeled by A-s Medication Solutions. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 50090-0617-0 100 tablet in 1 bottle, plastic , 50090-0617-1 30 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 Pnv Prenatal Plus Multivitamin?

To provide Vitamin and Mineral supplementation throughout pregnancy and during the postnatal period for both the lactating and non-lactating mother. It is also useful for improving nutritional status prior to conception.

Which are Pnv Prenatal Plus Multivitamin UNII Codes?

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

Which are Pnv Prenatal Plus Multivitamin 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".