Tretinoin NDC 46708-808

NDC codes

FDA NDC Directory

Product NDC (as listed)46708-808Labeler and product segments. Claims need a package NDC.

Product NDC at billing width46708-0808Add 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
46708-808-00	46708080800	1 TUBE in 1 CARTON (46708-808-00) / 45 g in 1 TUBEMarketed from Jun 11, 2026
46708-808-20	46708080820	1 TUBE in 1 CARTON (46708-808-20) / 20 g in 1 TUBEMarketed from Jun 11, 2026

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 — .5 mg/g
Dosage form: Cream
Route: Topical
Labeler: Alembic Pharmaceuticals Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 214590
Marketing start: Jun 11, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Retinoids (Chemical structure)
Identifiers: Product ID 46708-808_2fb4d13d-eeae-4605-adf6-41b96027b98cSPL ID 2fb4d13d-eeae-4605-adf6-41b96027b98cSPL set ID 5304df69-5d29-48f5-8227-80c7a6f12e6dRxCUI 106303UNII 5688UTC01RUPC 0346708808457
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

N446708080800 followed by a unit qualifier and the quantity

Package 46708-0808-00. 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 Jul 1, 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 214590

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

FDA NDC Directory listings under ANDA 214590
Product	Strength	Form · route	Labeler	Product NDC
Tretinoin	Tretinoin .5 mg/g	CreamTopical	Alembic Pharmaceuticals Inc.	62332-808