NDC codes

FDA NDC Directory
Product NDC (as listed)0093-5234Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00093-5234Add 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
0093-5234-56000935234560009352345630 TABLET, FILM COATED in 1 BOTTLE (0093-5234-56)Marketed from Oct 1, 2020

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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

Generic name (nonproprietary)
efavirenz, emtricitabine and tenofovir disoproxil fumarate
Active ingredients
Efavirenz — 600 mg/1Emtricitabine — 200 mg/1Tenofovir disoproxil fumarate — 300 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Teva Pharmaceuticals USA, Inc.NDC labeler code 0093
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091215
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 2B6 Inducers (Mechanism)Cytochrome P450 2C19 Inhibitors (Mechanism)Cytochrome P450 2C9 Inhibitors (Mechanism)Cytochrome P450 3A Inducers (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)Non-Nucleoside Analog (EXT)Non-Nucleoside Reverse Transcriptase Inhibitors (Mechanism)Nucleoside Reverse Transcriptase Inhibitors (Mechanism)Nucleoside Reverse Transcriptase Inhibitors (Mechanism)Nucleosides (Chemical structure)Nucleosides (Chemical structure)
Identifiers
Product ID 0093-5234_c1a1b151-9dea-485b-a42b-3483fb4ef7d7SPL ID c1a1b151-9dea-485b-a42b-3483fb4ef7d7SPL set ID fc9c2149-8d40-401b-af13-5ae7f953950aRxCUI 643066UNII JE6H2O27P8, G70B4ETF4S, OTT9J7900I
Pharmacologic class
Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor; Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor; Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase 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

N400093523456 followed by a unit qualifier and the quantity

Package 00093-5234-56. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Efavirenz, emtricitabine and tenofovir disoproxil fumarate tablets are indicated as a complete regimen or in combination with other antiretroviral agents for the treatment of HIV-1 infection in adults and pediatric patients weighing at least 40 kg. Efavirenz, emtricitabine and tenofovir disoproxil fumarate tablets are a three-drug combination of efavirenz (EFV), a non-nucleoside reverse transcriptase inhibitor, and emtricitabine (FTC) and tenofovir disoproxil fumarate (TDF), both HIV-1 nucleoside analog reverse transcriptase inhibitors, and is indicated as a complete regimen or in combination with other antiretroviral agents for the treatment of HIV-1 infection in adults and pediatric patien…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0093-5234

What is NDC 0093-5234?
0093-5234 is the product NDC for Efavirenz, Emtricitabine and Tenofovir Disoproxil Fumarate, Efavirenz 600 mg/1 + 2 more ingredients tablet, film coated, listed with the FDA by Teva Pharmaceuticals USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Efavirenz, Emtricitabine and Tenofovir Disoproxil Fumarate.
What is the active ingredient?
Efavirenz, Emtricitabine, Tenofovir disoproxil fumarate.
Who is the labeler?
Teva Pharmaceuticals USA, Inc., NDC labeler code 0093. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Efavirenz, Emtricitabine and Tenofovir Disoproxil Fumarate?
6 other product NDCs are listed under this name. See all Efavirenz, Emtricitabine and Tenofovir Disoproxil Fumarate 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 Efavirenz, Emtricitabine and Tenofovir Disoproxil Fumarate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Efavirenz, Emtricitabine and Tenofovir Disoproxil FumarateEfavirenz 600 mg/1 + 2 more ingredientsTablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-73631722-0736-30
Efavirenz, emtricitabine and tenofovir disoproxil fumarateEfavirenz 600 mg/1 + 2 more ingredientsTablet, Film coatedOralLaurus Labs Limited42385-91542385-0915-3042385-0915-90
Efavirenz, Emtricitabine and Tenofovir Disoproxil FumarateEfavirenz 600 mg/1 + 2 more ingredientsTablet, Film coatedOralMacleods Pharmaceuticals Limited33342-13833342-0138-07
Efavirenz, Emtricitabine And Tenofovir Disoproxil FumarateEfavirenz 600 mg/1 + 2 more ingredientsTablet, Film coatedOralAurobindo Pharma Limited65862-49765862-0497-30
efavirenz, emtricitabine and tenofovir disoproxil fumarateEfavirenz 600 mg/1 + 2 more ingredientsTablet, Film coatedOralCipla USA Inc.69097-21069097-0210-02
Efavirenz, Emtricitabine And Tenofovir Disoproxil FumarateEfavirenz 600 mg/1 + 2 more ingredientsTablet, Film coatedOralBryant Ranch Prepack72162-256572162-2565-03

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