NDC 0682-3001 Bacmin

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:
0682-3001
Proprietary Name:
Bacmin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Marnel Pharmaceuticals, Inc.
Labeler Code:
0682
Start Marketing Date: [9]
04-01-2000
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
RED (C48326 - DARK RED)
Shape:
OVAL (C48345)
Size(s):
19 MM
Imprint(s):
MMD
Score:
1

Product Packages

NDC Code 0682-3001-01

Package Description: 100 TABLET, COATED in 1 BOTTLE

Price per Unit: $0.68914 per EA

Product Details

What is NDC 0682-3001?

The NDC code 0682-3001 is assigned by the FDA to the product Bacmin which is product labeled by Marnel Pharmaceuticals, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0682-3001-01 100 tablet, coated 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 Bacmin?

This medication is a multivitamin product used to treat or prevent vitamin deficiency due to poor diet, certain illnesses, or during pregnancy. Vitamins are important building blocks of the body and help keep you in good health.

Which are Bacmin UNII Codes?

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

Which are Bacmin 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:

* 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".