Tretinoin NDC 62332-809

NDC codes

FDA NDC Directory

Product NDC (as listed)62332-809Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62332-0809Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
62332-809-20	62332080920	1 TUBE in 1 CARTON (62332-809-20) / 20 g in 1 TUBEMarketed from Aug 16, 2025
62332-809-45	62332080945	1 TUBE in 1 CARTON (62332-809-45) / 45 g in 1 TUBEMarketed from Aug 16, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Tretinoin
Generic name (nonproprietary): tretinoin
Active ingredients: Tretinoin — .25 mg/g
Dosage form: Cream
Route: Topical
Labeler: Alembic Pharmaceuticals Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218399
Marketing start: Aug 16, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Retinoids (Chemical structure)
Identifiers: Product ID 62332-809_942c8089-c604-46d6-929d-3c2b07f00d39SPL ID 942c8089-c604-46d6-929d-3c2b07f00d39SPL set ID 872b3f8f-c073-4808-a106-840188ac7a00RxCUI 106302UNII 5688UTC01RUPC 0362332809455, 0362332809202
Pharmacologic class: Retinoid

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N462332080920 followed by a unit qualifier and the quantity

Package 62332-0809-20. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 23, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Tretinoin Cream is indicated for topical application in the treatment of acne vulgaris. The safety and efficacy of the long-term use of this product in the treatment of other disorders have not been established.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 218399

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 218399
Product	Strength	Form · route	Labeler	Product NDC
Tretinoin	Tretinoin .25 mg/g	CreamTopical	Alembic Pharmaceuticals Limited	46708-809