70529-049 NDC - CORVATROL 0.9% ()

Drug Information

  • Product NDC: 70529-049
  • Proprietary Name: Corvatrol 0.9%
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: IT3 Medical LLC
Product Type:
FDA Application Number: ANDA088911
Marketing Category: ANDA
Start Marketing Date:3/1/2017

Package Information

No. Package Code Package Description Billing Unit
170529-049-011 VIAL, MULTI-DOSE in 1 PACKAGE (70529-049-01) / 30 mL in 1 VIAL, MULTI-DOSE
270529-049-151 VIAL, MULTI-DOSE in 1 PACKAGE (70529-049-15) / 10 mL in 1 VIAL, MULTI-DOSE
370529-049-202 VIAL, MULTI-DOSE in 1 PACKAGE (70529-049-20) / 30 mL in 1 VIAL, MULTI-DOSE
470529-049-252 VIAL, MULTI-DOSE in 1 PACKAGE (70529-049-25) / 10 mL in 1 VIAL, MULTI-DOSE
570529-049-303 VIAL, MULTI-DOSE in 1 PACKAGE (70529-049-30) / 30 mL in 1 VIAL, MULTI-DOSE
670529-049-353 VIAL, MULTI-DOSE in 1 PACKAGE (70529-049-35) / 10 mL in 1 VIAL, MULTI-DOSE
770529-049-404 VIAL, MULTI-DOSE in 1 PACKAGE (70529-049-40) / 30 mL in 1 VIAL, MULTI-DOSE
870529-049-454 VIAL, MULTI-DOSE in 1 PACKAGE (70529-049-45) / 10 mL in 1 VIAL, MULTI-DOSE

NDC Record

Field Name Field Value Definition
PRODUCT NDC70529-049The 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.
PROPRIETARY NAMECorvatrol 0.9%The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/1/2017This 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 NUMBERANDA088911This 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 NAMEIT3 Medical LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/6/2025

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