NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1933Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1933Add 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 NDC11-digit (billing)PackageCopy
70771-1933-2707711933021 TUBE in 1 CARTON (70771-1933-2) / 20 g in 1 TUBEMarketed from Oct 1, 2026
70771-1933-4707711933041 TUBE in 1 CARTON (70771-1933-4) / 45 g in 1 TUBEMarketed from Oct 1, 2026

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
Zydus Lifesciences LimitedNDC labeler code 70771
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218560
Marketing start
Listing expires
Other FDA classes
Retinoids (Chemical structure)
Identifiers
Product ID 70771-1933_1df91300-7a8d-4354-8451-512247804a71SPL ID 1df91300-7a8d-4354-8451-512247804a71
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

N470771193302 followed by a unit qualifier and the quantity

Package 70771-1933-02. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70771-1933

What is NDC 70771-1933?
70771-1933 is the product NDC for Tretinoin, Tretinoin .25 mg/g cream, listed with the FDA by Zydus Lifesciences Limited. 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?
Zydus Lifesciences Limited, NDC labeler code 70771. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
TretinoinTretinoin .25 mg/gCreamTopicalViona Pharmaceuticals Inc72578-15572578-0155-0872578-0155-09
TretinoinTretinoin .5 mg/gCreamTopicalAlembic Pharmaceuticals Limited46708-80846708-0808-0046708-0808-20
TretinoinTretinoin .5 mg/gCreamTopicalAlembic Pharmaceuticals Inc.62332-80862332-0808-2062332-0808-45
TretinoinTretinoin .8 mg/gGelTopicalAmneal Pharmaceuticals NY LLC69238-232369238-2323-01
TretinoinTretinoin .6 mg/gGelTopicalEncube Ethicals, Inc.21922-04221922-0042-40
TretinoinTretinoin .5 mg/gCreamTopicalEncube Ethicals, Inc.21922-07821922-0078-0621922-0078-25
TretinoinTretinoin 1 mg/gCreamTopicalEncube Ethicals, Inc.21922-07721922-0077-0621922-0077-25
TretinoinTretinoin .25 mg/gCreamTopicalPreferred Pharmaceuticals Inc.68788-406968788-4069-02
TretinoinTretinoin .25 mg/gCreamTopicalAlembic Pharmaceuticals Limited46708-80946708-0809-2046708-0809-45
TretinoinTretinoin .25 mg/gCreamTopicalAlembic Pharmaceuticals Inc.62332-80962332-0809-2062332-0809-45

All 69 Tretinoin NDCs

Other NDCs under ANDA 218560

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

FDA NDC Directory listings under ANDA 218560
ProductStrengthForm · routeLabelerProduct NDC
TretinoinTretinoin .25 mg/gCreamTopicalViona Pharmaceuticals Inc72578-155

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