NDC directory

Tretinoin

Viona Pharmaceuticals Inc · CREAM

72578-155ANDARetinoid [EPC]
Product NDC
72578-155
Generic name
Tretinoin
Labeler name
Viona Pharmaceuticals Inc
Brand name
Tretinoin
Finished
true
Listing expiration date
20271231
Marketing category
ANDA
Dosage form
CREAM
SPL ID
22150db5-d543-419f-bc09-a3280e19777b
Product type
HUMAN PRESCRIPTION DRUG
Marketing start date
20261001
Product ID
72578-155_22150db5-d543-419f-bc09-a3280e19777b
Application number
ANDA218560
Brand name base
Tretinoin
Active ingredients
  1. Name
    TRETINOIN
    Strength
    .25 mg/g
Packaging
  1. Package NDC
    72578-155-08
    Description
    1 TUBE in 1 CARTON (72578-155-08) / 45 g in 1 TUBE
    Marketing start date
    20261001
    Sample
    false
  2. Package NDC
    72578-155-09
    Description
    1 TUBE in 1 CARTON (72578-155-09) / 20 g in 1 TUBE
    Marketing start date
    20261001
    Sample
    false
Route
TOPICAL
Pharm class
Retinoid [EPC], Retinoids [CS]
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.