NDC Package 14335-150-01 Acyclovir Sodium

Powder - View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
14335-150-01
Package Description:
8 kg in 1 DRUM
Product Code:
Non-Proprietary Name:
Acyclovir Sodium
Substance Name:
Acyclovir Sodium
Usage Information:
This medication is used in certain people to treat outbreaks of herpes simplex infection of the skin (such as on the genitals), mucous membrane areas (such as the mouth, nose), or brain. It is also used in certain people to treat shingles infection. The viruses that cause these infections live in the body quietly until an outbreak occurs. Acyclovir does not cure these infections, but can speed healing of the sores, decrease pain/itching/formation of new sores, and lower the risk of other problems from the virus (e.g., infection spreading to other parts of the body/organs, persistent pain after sores heal).
11-Digit NDC Billing Format:
14335015001
Product Type:
Bulk Ingredient
Labeler Name:
Hainan Poly Pharm. Co., Ltd.
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Active Ingredient(s):
Sample Package:
N/A
Marketing Category:
BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
Start Marketing Date:
12-10-2021
Listing Expiration Date:
12-31-2024
Exclude Flag:
N
Unfinished Product:
Yes
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.

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Frequently Asked Questions

What is NDC 14335-150-01?

The NDC Packaged Code 14335-150-01 is assigned to an UNFINISHED drug package of 8 kg in 1 drum of Acyclovir Sodium, a bulk ingredient labeled by Hainan Poly Pharm. Co., Ltd.. The product's dosage form is powder and is administered via form.

Is NDC 14335-150 included in the NDC Directory?

Yes, Acyclovir Sodium is an UNFINISHED PRODUCT with code 14335-150 that is active and included in the NDC Directory. The product was first marketed by Hainan Poly Pharm. Co., Ltd. on December 10, 2021 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 14335-150-01?

The 11-digit format is 14335015001. 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 5-3-2 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
5-3-214335-150-015-4-214335-0150-01