NDC codes

FDA NDC Directory
Product NDC (as listed)60219-1145Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60219-1145Add 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
60219-1145-360219114503602191145031 BOTTLE, PLASTIC in 1 CARTON (60219-1145-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Dec 9, 2023

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)
Darunavir
Generic name (nonproprietary)
darunavir
Active ingredients
Darunavir — 800 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Amneal Pharmaceuticals NY LLCNDC labeler code 60219
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212493
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 2D6 Inhibitors (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)HIV Protease Inhibitors (Mechanism)
Identifiers
Product ID 60219-1145_7fb8acac-13ca-47ca-8b06-d12900d4943bSPL ID 7fb8acac-13ca-47ca-8b06-d12900d4943bSPL set ID 92b286d5-1ee5-435b-9e1d-2e95c7f2ec69RxCUI 670026, 1359269UNII YO603Y8113UPC 0360219114463, 0360219114531
Pharmacologic class
Protease Inhibitor

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

N460219114503 followed by a unit qualifier and the quantity

Package 60219-1145-03. 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 .

Indications (excerpt from the label)

Darunavir, co-administered with ritonavir (darunavir/ritonavir), in combination with other antiretroviral agents, is indicated for the treatment of human immunodeficiency virus (HIV-1) infection in adult and pediatric patients 3 years of age and older [see Use in Specific Populations (8.4) and Clinical Studies (14) ] . Darunavir is a human immunodeficiency virus (HIV-1) protease inhibitor indicated for the treatment of HIV-1 infection in adult and pediatric patients 3 years of age and older. Darunavir tablets must be co-administered with ritonavir (darunavir/ritonavir) and with other antiretroviral agents. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60219-1145

What is NDC 60219-1145?
60219-1145 is the product NDC for Darunavir, Darunavir 800 mg/1 tablet, film coated, listed with the FDA by Amneal Pharmaceuticals NY LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Darunavir.
What is the active ingredient?
Darunavir.
Who is the labeler?
Amneal Pharmaceuticals NY LLC, NDC labeler code 60219. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Darunavir?
23 other product NDCs are listed under this name. See all Darunavir 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 Darunavir NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
DarunavirDarunavir 600 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-08831722-0088-60
DarunavirDarunavir 800 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-08931722-0089-30
DarunavirDarunavir dihydrate 800 mg/1TabletOralAmerican Health Packaging60687-81960687-0819-21
DarunavirDarunavir dihydrate 600 mg/1TabletOralAmerican Health Packaging60687-80860687-0808-21
DarunavirDarunavir 600 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-174570771-1745-0570771-1745-0670771-1745-08
DarunavirDarunavir 800 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-174670771-1746-0370771-1746-0570771-1746-09
DarunavirDarunavir 600 mg/1Tablet, Film coatedOralViona Pharmaceuticals Inc72578-14772578-0147-0572578-0147-1472578-0147-28
DarunavirDarunavir 800 mg/1Tablet, Film coatedOralViona Pharmaceuticals Inc72578-14872578-0148-0572578-0148-0672578-0148-16
darunavirdarunavir 600 mgDarunavir hydrate 600 mg/1TabletOralEXELAN PHARMACEUTICALS INC.76282-73776282-0737-60
darunavirdarunavir 800 mgDarunavir hydrate 800 mg/1TabletOralEXELAN PHARMACEUTICALS INC.76282-73876282-0738-30

All 24 Darunavir NDCs

Other NDCs under ANDA 212493

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

FDA NDC Directory listings under ANDA 212493
ProductStrengthForm · routeLabelerProduct NDC
DarunavirDarunavir 600 mg/1Tablet, Film coatedOralAmneal Pharmaceuticals NY LLC60219-1144

Free account

Log in to keep searching

You’ve used your 3 free searches. Med-Code is free: log in or create a free profile to keep looking up NDCs, J-codes and drugs.

Create a free profileLog in