NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1075Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1075Add 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
70771-1075-070771107500707711075001000 CAPSULE, COATED PELLETS in 1 BOTTLE (70771-1075-0)Marketed from Jun 8, 2017
70771-1075-17077110750170771107501100 CAPSULE, COATED PELLETS in 1 BOTTLE (70771-1075-1)Marketed from Jun 8, 2017
70771-1075-3707711075037077110750330 CAPSULE, COATED PELLETS in 1 BOTTLE (70771-1075-3)Marketed from Jun 8, 2017
70771-1075-4707711075047077110750410 BLISTER PACK in 1 CARTON (70771-1075-4) / 10 CAPSULE, COATED PELLETS in 1 BLISTER PACKMarketed from Jun 8, 2017
70771-1075-57077110750570771107505500 CAPSULE, COATED PELLETS in 1 BOTTLE (70771-1075-5)Marketed from Jun 8, 2017
70771-1075-9707711075097077110750990 CAPSULE, COATED PELLETS in 1 BOTTLE (70771-1075-9)Marketed from Jun 8, 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)
budesonide
Generic name (nonproprietary)
budesonide
Active ingredients
Budesonide — 3 mg/1
Dosage form
Capsule, Coated pellets
Route
Oral
Labeler
Zydus Lifesciences LimitedNDC labeler code 70771
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206134
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 70771-1075_bfde9c2e-2ff5-4258-91bc-78a48b228d14SPL ID bfde9c2e-2ff5-4258-91bc-78a48b228d14SPL set ID d645a346-c99b-4de7-9bca-69e73266d6b4RxCUI 1244214UNII Q3OKS62Q6XUPC 0368382720016
Pharmacologic class
Corticosteroid

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

N470771107500 followed by a unit qualifier and the quantity

Package 70771-1075-00. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 70771-1075

What is NDC 70771-1075?
70771-1075 is the product NDC for budesonide, Budesonide 3 mg/1 capsule, coated pellets, listed with the FDA by Zydus Lifesciences Limited. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
budesonide.
What is the active ingredient?
Budesonide.
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 budesonide?
41 other product NDCs are listed under this name. See all budesonide 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 budesonide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
BudesonideBudesonide .25 mg/2mLSuspensionRespiratory (Inhalation)American Health Packaging60687-88960687-0889-83
budesonideBudesonide 3 mg/1Capsule, Coated pelletsOralREMEDYREPACK INC.70518-461370518-4613-00
BudesonideBudesonide 32 ug/1Spray, MeteredNasalRugby Laboratories0536-145600536-1456-84
BudesonideBudesonide 32 ug/1Spray, MeteredNasalWalgreens0363-004800363-0048-01
BudesonideBudesonide 32 ug/1Spray, MeteredNasalEQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)49035-70349035-0703-01
BudesonideBudesonide 32 ug/1Spray, MeteredNasalCVS Pharmacy69842-00169842-0001-01
BudesonideBudesonide 3 mg/1Capsule, Delayed releaseOralAmneal Pharmaceuticals of New York LLC53746-77853746-0778-10
BudesonideBudesonide .25 mg/2mLInhalantRespiratory (Inhalation)Rising Pharma Holdings, Inc.64980-63864980-0638-03
BudesonideBudesonide .5 mg/2mLInhalantRespiratory (Inhalation)Rising Pharma Holdings, Inc.64980-63964980-0639-03
budesonideBudesonide 3 mg/1Capsule, Coated pelletsOralMajor Pharmaceuticals0904-731300904-7313-10

All 42 budesonide NDCs

Other NDCs under ANDA 206134

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

FDA NDC Directory listings under ANDA 206134
ProductStrengthForm · routeLabelerProduct NDC
budesonideBudesonide 3 mg/1Capsule, Coated pelletsOralMajor Pharmaceuticals0904-7313
budesonideBudesonide 3 mg/1Capsule, Coated pelletsOralNorthstar Rx LLC.16714-829
BudesonideBudesonide 3 mg/1Capsule, Coated pelletsOralAmerican Health Packaging60687-596
budesonideBudesonide 3 mg/1Capsule, Coated pelletsOralZydus Pharmaceuticals USA Inc.68382-720
budesonideBudesonide 3 mg/1Capsule, Coated pelletsOralREMEDYREPACK INC.70518-4613

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