69054-211 NDC - OCUVEL ()

Drug Information

  • Product NDC: 69054-211
  • Proprietary Name: Ocuvel
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Adler-Stern Pharmaceuticals, LLC
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:12/1/2014

Package Information

No. Package Code Package Description Billing Unit
169054-211-6060 CAPSULE in 1 BOTTLE, PLASTIC (69054-211-60)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC69054-211The 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 NAMEOcuvelIndicates 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.
START MARKETING DATE12/1/2014The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
LABELER NAMEAdler-Stern Pharmaceuticals, LLCThe translation of the dosage form Code submitted by the firm.

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This page was last updated on: 1/16/2026

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