NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1662Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1662Add 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
70771-1662-870771166208707711662083 BLISTER PACK in 1 CARTON (70771-1662-8) / 10 CAPSULE in 1 BLISTER PACK (70771-1662-2)Marketed from Jun 9, 2025

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)
Isotretinoin
Generic name (nonproprietary)
isotretinoin
Active ingredients
Isotretinoin — 10 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Zydus Lifesciences LimitedNDC labeler code 70771
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216633
Marketing start
Listing expires
Other FDA classes
Retinoids (Chemical structure)
Identifiers
Product ID 70771-1662_26618883-d91c-476e-b22c-4d0e204b9dd3SPL ID 26618883-d91c-476e-b22c-4d0e204b9dd3SPL set ID 245898e5-3a61-4d6a-8375-8b3a8b7364acRxCUI 197843, 197844, 197845, 403930, 1547561, 1547565UNII EH28UP18IF
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470771166208 followed by a unit qualifier and the quantity

Package 70771-1662-08. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 70771-1662

What is NDC 70771-1662?
70771-1662 is the product NDC for Isotretinoin, Isotretinoin 10 mg/1 capsule, listed with the FDA by Zydus Lifesciences Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Isotretinoin.
What is the active ingredient?
Isotretinoin.
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 Isotretinoin?
66 other product NDCs are listed under this name. See all Isotretinoin 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 Isotretinoin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
IsotretinoinIsotretinoin 20 mg/1CapsuleOralAurobindo Pharma Limited84386-00984386-0009-03
IsotretinoinIsotretinoin 30 mg/1CapsuleOralAurobindo Pharma Limited84386-01084386-0010-03
IsotretinoinIsotretinoin 40 mg/1CapsuleOralAurobindo Pharma Limited84386-01184386-0011-03
IsotretinoinIsotretinoin 10 mg/1CapsuleOralAmneal Pharmaceuticals NY LLC69238-125469238-1254-03
IsotretinoinIsotretinoin 20 mg/1CapsuleOralAmneal Pharmaceuticals NY LLC69238-125569238-1255-03
IsotretinoinIsotretinoin 25 mg/1CapsuleOralAmneal Pharmaceuticals NY LLC69238-125669238-1256-03
IsotretinoinIsotretinoin 30 mg/1CapsuleOralAmneal Pharmaceuticals NY LLC69238-125769238-1257-03
IsotretinoinIsotretinoin 35 mg/1CapsuleOralAmneal Pharmaceuticals NY LLC69238-125869238-1258-03
IsotretinoinIsotretinoin 40 mg/1CapsuleOralAmneal Pharmaceuticals NY LLC69238-125969238-1259-03
IsotretinoinIsotretinoin 10 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-157470710-1574-08

All 67 Isotretinoin NDCs

Other NDCs under ANDA 216633

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

FDA NDC Directory listings under ANDA 216633
ProductStrengthForm · routeLabelerProduct NDC
IsotretinoinIsotretinoin 20 mg/1CapsuleOralZydus Lifesciences Limited70771-1663
IsotretinoinIsotretinoin 40 mg/1CapsuleOralZydus Lifesciences Limited70771-1667
IsotretinoinIsotretinoin 25 mg/1CapsuleOralZydus Lifesciences Limited70771-1664
IsotretinoinIsotretinoin 30 mg/1CapsuleOralZydus Lifesciences Limited70771-1665
IsotretinoinIsotretinoin 35 mg/1CapsuleOralZydus Lifesciences Limited70771-1666
IsotretinoinIsotretinoin 10 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1574
IsotretinoinIsotretinoin 35 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1578
IsotretinoinIsotretinoin 20 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1575
IsotretinoinIsotretinoin 25 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1576
IsotretinoinIsotretinoin 30 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1577
IsotretinoinIsotretinoin 40 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1579

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