68382-747 NDC - TIADYLT ER (DILTIAZEM HYDROCHLORIDE)

Drug Information

Product NDC: 68382-747

Proprietary Name: TIADYLT ER

Non Proprietary Name: diltiazem hydrochloride

Active Ingredient(s):
  • 240 mg/1 DILTIAZEM HYDROCHLORIDE


Administration Route(s): ORAL

Dosage Form(s): CAPSULE, EXTENDED RELEASE

Pharmacy Class(es):
  • Calcium Channel Antagonists [MoA];
  • Calcium Channel Blocker [EPC]

Labeler Information

Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA206641
Marketing Category: ANDA
Start Marketing Date:11/8/2017

Package Information

No. Package Code Package Description Billing Unit
168382-747-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-747-01)
268382-747-05500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-747-05)
368382-747-0630 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-747-06)
468382-747-101000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-747-10)
568382-747-1690 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-747-16)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68382-747The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMETIADYLT ERThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEdiltiazem hydrochlorideThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECAPSULE, EXTENDED RELEASEThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE11/8/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERANDA206641This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEZydus Pharmaceuticals (USA) Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEDILTIAZEM HYDROCHLORIDEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH240 
ACTIVE INGRED UNITmg/1 
PHARM CLASSESCalcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] 

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This page was last updated on: 8/16/2019