NDC 21695-403 Diltiazem Hydrochloride

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:
21695-403
Proprietary Name:
Diltiazem Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rebel Distributors Corp
Labeler Code:
21695
Start Marketing Date: [9]
12-20-1999
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GRAY (C48324 - LIGHT GRAY OPAQUE)
Shape:
CAPSULE (C48336)
Size(s):
18 MM
Imprint(s):
R2588
Score:
1

Product Packages

NDC Code 21695-403-30

Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE

Product Details

What is NDC 21695-403?

The NDC code 21695-403 is assigned by the FDA to the product Diltiazem Hydrochloride which is product labeled by Rebel Distributors Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 21695-403-30 30 capsule, extended release 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 Diltiazem Hydrochloride?

Diltiazem hydrochloride extended-release capsules are indicated for the treatment of hypertension. They may be used alone or in combination with other antihypertensive medications.Diltiazem hydrochloride extended-release capsules are indicated for the management of chronic stable angina and angina due to coronary artery spasm.

Which are Diltiazem Hydrochloride UNII Codes?

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

Which are Diltiazem Hydrochloride 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:

What is the NDC to RxNorm Crosswalk for Diltiazem Hydrochloride?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 830837 - dilTIAZem HCl 240 MG 24HR Extended Release Oral Capsule
  • RxCUI: 830837 - 24 HR diltiazem hydrochloride 240 MG Extended Release Oral Capsule
  • RxCUI: 830837 - diltiazem HCl 240 MG 24 HR Extended Release Oral Capsule
  • RxCUI: 830845 - dilTIAZem HCl 180 MG 24HR Extended Release Oral Capsule
  • RxCUI: 830845 - 24 HR diltiazem hydrochloride 180 MG Extended Release Oral Capsule

* 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".