What is NDC 72162-2135?

72162-2135 is the product NDC for Tretinoin, Tretinoin .25 mg/g cream, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Tretinoin?

68 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Tretinoin NDC 72162-2135 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-2135Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-2135Add 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
72162-2135-2	7216221350272162213502	1 TUBE in 1 CARTON (72162-2135-2) / 20 g in 1 TUBEMarketed from Jun 15, 2017
72162-2135-4	7216221350472162213504	1 TUBE in 1 CARTON (72162-2135-4) / 45 g in 1 TUBEMarketed from Jun 15, 2017

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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: Bryant Ranch PrepackNDC labeler code 72162
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075264
Marketing start: Jun 15, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Retinoids (Chemical structure)
Identifiers: Product ID 72162-2135_5e84c976-d4d6-4d8f-a448-8afb47e2fbffSPL ID 5e84c976-d4d6-4d8f-a448-8afb47e2fbffSPL set ID 5e84c976-d4d6-4d8f-a448-8afb47e2fbffRxCUI 106302UNII 5688UTC01R
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

N472162213502 followed by a unit qualifier and the quantity

Package 72162-2135-02. 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 Apr 3, 2024.

Indications (excerpt from the label)

Indications and Usage: Tretinoin gel and cream are 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)

About NDC 72162-2135

What is NDC 72162-2135?: 72162-2135 is the product NDC for Tretinoin, Tretinoin .25 mg/g cream, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Tretinoin.
What is the active ingredient?: Tretinoin.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Tretinoin?: 68 other product NDCs are listed under this name. See all Tretinoin NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Tretinoin NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Tretinoin	Tretinoin .25 mg/g	CreamTopical	Zydus Lifesciences Limited	70771-1933	70771-1933-0270771-1933-04
Tretinoin	Tretinoin .25 mg/g	CreamTopical	Viona Pharmaceuticals Inc	72578-155	72578-0155-0872578-0155-09
Tretinoin	Tretinoin .5 mg/g	CreamTopical	Alembic Pharmaceuticals Limited	46708-808	46708-0808-0046708-0808-20
Tretinoin	Tretinoin .5 mg/g	CreamTopical	Alembic Pharmaceuticals Inc.	62332-808	62332-0808-2062332-0808-45
Tretinoin	Tretinoin .8 mg/g	GelTopical	Amneal Pharmaceuticals NY LLC	69238-2323	69238-2323-01
Tretinoin	Tretinoin .6 mg/g	GelTopical	Encube Ethicals, Inc.	21922-042	21922-0042-40
Tretinoin	Tretinoin .5 mg/g	CreamTopical	Encube Ethicals, Inc.	21922-078	21922-0078-0621922-0078-25
Tretinoin	Tretinoin 1 mg/g	CreamTopical	Encube Ethicals, Inc.	21922-077	21922-0077-0621922-0077-25
Tretinoin	Tretinoin .25 mg/g	CreamTopical	Preferred Pharmaceuticals Inc.	68788-4069	68788-4069-02
Tretinoin	Tretinoin .25 mg/g	CreamTopical	Alembic Pharmaceuticals Limited	46708-809	46708-0809-2046708-0809-45

All 69 Tretinoin NDCs

Other NDCs under ANDA 075264

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

FDA NDC Directory listings under ANDA 075264
Product	Strength	Form · route	Labeler	Product NDC
Tretinoin	Tretinoin .25 mg/g	CreamTopical	Padagis US LLC	0574-2225
Tretinoin	Tretinoin .25 mg/g	CreamTopical	A-S Medication Solutions	50090-3128
Tretinoin	Tretinoin .25 mg/g	CreamTopical	NuCare Pharmaceuticals,Inc.	68071-3945
Tretinoin	Tretinoin .25 mg/g	CreamTopical	Preferred Pharmaceuticals Inc.	68788-4069