NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1139Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1139Add 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
70771-1139-170771113901100 TABLET in 1 BOTTLE (70771-1139-1)Marketed from Dec 2, 2017
70771-1139-570771113905500 TABLET in 1 BOTTLE (70771-1139-5)Marketed from Dec 2, 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)
Azathioprine
Generic name (nonproprietary)
azathioprine
Active ingredients
Azathioprine — 25 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077621
Marketing start
Listing expires
Other FDA classes
Nucleic Acid Synthesis Inhibitors (Mechanism)Nucleosides (Chemical structure)Purines (Chemical structure)
Identifiers
Product ID 70771-1139_1277f50f-59f8-4c65-88de-011424884c3bSPL ID 1277f50f-59f8-4c65-88de-011424884c3bSPL set ID 89b272f0-ef5c-49e4-820f-fcd7ea8ef066RxCUI 199310, 359228, 359229UNII MRK240IY2L
Pharmacologic class
Purine Antimetabolite

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

N470771113901 followed by a unit qualifier and the quantity

Package 70771-1139-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 077621

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

FDA NDC Directory listings under ANDA 077621
ProductStrengthForm · routeLabelerProduct NDC
AzathioprineAzathioprine 50 mg/1TabletOralAmerican Health Packaging68084-229
AzathioprineAzathioprine 75 mg/1TabletOralZydus Lifesciences Limited70771-1140
AzathioprineAzathioprine 100 mg/1TabletOralZydus Lifesciences Limited70771-1141
AzathioprineAzathioprine 50 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-003
AzathioprineAzathioprine 25 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-118
AzathioprineAzathioprine 75 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-119
AzathioprineAzathioprine 100 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-120
AzathioprineAzathioprine 50 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3772
AzathioprineAzathioprine 50 mg/1TabletOralZydus Lifesciences Limited65841-602

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