Tretinoin 0.25 mg / g Gel 1 Tube

Reference details for licensed healthcare facility review and verification.

NDC 1171335-2898-01
Product NDC71335-2898
Generic Drug NameTretinoin
Brand NameTretinoin
ManufacturerBryant Ranch Prepack
Strength0.25 mg / g
Dosage FormGel
Drug TypeTopical
Package Quantity1 Tube
Package Description1 TUBE in 1 CARTON (71335-2898-1) / 45 g in 1 TUBE
Active IngredientsTretinoin
Marketing CategoryNDA AUTHORIZED GENERIC

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NDC snapshot

Tretinoin 0.25 mg / g Gel is tracked under NDC 71335-2898-01 and rolls up into product family 71335-2898. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 1 Tube.
  • Manufacturer: Bryant Ranch Prepack.
  • Dosage form: Gel.
  • Family size: 1 indexed presentation.

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Official references

Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.

Potential alternatives with matching presentation

Open the comparison hub or review package-level listings from 6 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.

View Potential Alternative Hubtretinoin 0.25 mg / g Gel 1 Tube Tube11 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Tretinoin 0.25 mg / g Gel 1 Tube, NDC 71335-2898-01, is a Bryant Ranch Prepack 0.25 mg / g gel presentation packaged as 1 Tube.

NDC search formats

  • Canonical NDC 11: 71335-2898-01
  • Digits-only NDC 11: 71335289801
  • Possible 10-digit display format: 71335-2898-1 (7133528981)

Helpful product links

  • Search by brand name: Tretinoin
  • NDC 11: 71335-2898-01
  • Product family NDC: 71335-2898
  • VA classification code: DE752
  • VA classification code description: ANTIACNE AGENTS,TOPICAL
  • CMOP ID: T0084
  • VUID: 4005218