NDC Package 0642-0070-30 Vitafol One

Prenatal Supplement With Dha Capsule, Gelatin Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0642-0070-30
Package Description:
5 BLISTER PACK in 1 BOX / 6 CAPSULE, GELATIN COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Vitafol One
Non-Proprietary Name:
Prenatal Supplement With Dha
Substance Name:
.alpha.-tocopherol; Ascorbic Acid; Copper; Cyanocobalamin; Folic Acid; Iodine; Iron; Magnesium; Niacin; Omega-3 Fatty Acids; Pyridoxine Hydrochloride; Riboflavin; Thiamine Mononitrate; Vitamin A; Vitamin D; Zinc
Usage Information:
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.
11-Digit NDC Billing Format:
00642007030
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
5 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1119569 - ascorbic acid 30 MG / cholecalciferol 1000 UNT / cuprous oxide 2 MG / folic acid 1 MG / magnesium oxide 20 MG / niacin 15 MG / polysaccharide iron complex 29 MG / potassium iodide 0.15 MG / pyridoxine hydrochloride 2.5 MG / riboflavin 1.8 MG / thiamine mononitrate 1.6 MG / vitamin A 1100 UNT / vitamin B12 0.012 MG / vitamin E 20 UNT / zinc oxide 25 MG Oral Capsule
  • RxCUI: 1119569 - vitamin C 30 MG / cholecalciferol 1000 UNT / cuprous oxide 2 MG / folate 1 MG / magnesium oxide 20 MG / nicotinic acid 15 MG / polysaccharide iron complex 29 MG / K+ iodide 0.15 MG / vitamin B6 hydrochloride 2.5 MG / riboflavin 1.8 MG / vitamin B1 mononitrate 1.6 MG / vitamin A 1100 UNT / vitamin B12 0.012 MG / vitamin E 20 UNT / ZNO 25 MG Oral Capsule
  • RxCUI: 1119569 - vitamin C 30 MG / cholecalciferol 1000 UNT / cuprous oxide 2 MG / folate 1 MG / magnesium oxide 20 MG / nicotinic acid 15 MG / polysaccharide iron complex 29 MG / K+ iodide 0.15 MG / vitamin B6 hydrochloride 2.5 MG / riboflavin 1.8 MG / vit-B1 mononitrate 1.6 MG / vitamin A 1100 UNT / vitamin B12 0.012 MG / vitamin E 20 UNT / ZNO 25 MG Oral Capsule
  • RxCUI: 1119569 - vitamin C 30 MG / cholecalciferol 1000 UNT / cuprous oxide 2 MG / folate 1 MG / magnesium oxide 20 MG / nicotinic acid 15 MG / polysaccharide iron complex 29 MG / K+ iodide 0.15 MG / vit-B6 hydrochloride 2.5 MG / riboflavin 1.8 MG / vitamin B1 mononitrate 1.6 MG / vitamin A 1100 UNT / vitamin B12 0.012 MG / vitamin E 20 UNT / ZNO 25 MG Oral Capsule
  • RxCUI: 1119569 - vitamin C 30 MG / cholecalciferol 1000 UNT / cuprous oxide 2 MG / folate 1 MG / magnesium oxide 20 MG / nicotinic acid 15 MG / polysaccharide iron complex 29 MG / K+ iodide 0.15 MG / vit-B6 hydrochloride 2.5 MG / riboflavin 1.8 MG / vit-B1 mononitrate 1.6 MG / vitamin A 1100 UNT / vitamin B12 0.012 MG / vitamin E 20 UNT / ZNO 25 MG Oral Capsule
Product Type:
Human Prescription Drug
Labeler Name:
Exeltis Usa, Inc.
Dosage Form:
Capsule, Gelatin Coated - A solid dosage form in which the drug is enclosed within either a hard or soft soluble container made from a suitable form of gelatin; through a banding process, the capsule is coated with additional layers of gelatin so as to form a complete seal.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
Marketing Category:
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date:
06-13-2011
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
0642-0070-011 BLISTER PACK in 1 BOX / 4 CAPSULE, GELATIN COATED in 1 BLISTER PACK
0642-0070-031 BLISTER PACK in 1 BOX / 3 CAPSULE, GELATIN COATED in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0642-0070-30?

The NDC Packaged Code 0642-0070-30 is assigned to a package of 5 blister pack in 1 box / 6 capsule, gelatin coated in 1 blister pack of Vitafol One, a human prescription drug labeled by Exeltis Usa, Inc.. The product's dosage form is capsule, gelatin coated and is administered via oral form.

Is NDC 0642-0070 included in the NDC Directory?

Yes, Vitafol One with product code 0642-0070 is active and included in the NDC Directory. The product was first marketed by Exeltis Usa, Inc. on June 13, 2011 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0642-0070-30?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 5.

What is the 11-digit format for NDC 0642-0070-30?

The 11-digit format is 00642007030. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
4-4-20642-0070-305-4-200642-0070-30