NDC codes

FDA NDC Directory
Product NDC (as listed)59651-166Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59651-0166Add 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
59651-166-30596510166305965101663030 TABLET, FILM COATED in 1 BOTTLE (59651-166-30)Marketed from Mar 9, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
emtricitabine and tenofovir disoproxil fumarate
Active ingredients
Emtricitabine — 133 mg/1Tenofovir disoproxil fumarate — 200 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Aurobindo Pharma LimitedNDC labeler code 59651
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211640
Marketing start
Listing expires
Other FDA classes
Nucleoside Reverse Transcriptase Inhibitors (Mechanism)Nucleoside Reverse Transcriptase Inhibitors (Mechanism)Nucleosides (Chemical structure)Nucleosides (Chemical structure)
Identifiers
Product ID 59651-166_a805c27a-1154-4aac-9af8-bbd755be027fSPL ID a805c27a-1154-4aac-9af8-bbd755be027fSPL set ID 974d2ec8-1b51-4e69-991d-0d5dea8360f4RxCUI 1744001, 1744005, 1744009UNII G70B4ETF4S, OTT9J7900I
Pharmacologic class
Hepatitis B Virus 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

N459651016630 followed by a unit qualifier and the quantity

Package 59651-0166-30. 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)

HIV-1 Treatment ( 1.1 ) Emtricitabine and tenofovir disoproxil fumarate tablets are a two-drug combination of emtricitabine (FTC) and tenofovir disoproxil fumarate (TDF), both HIV-1 nucleoside analog reverse transcriptase inhibitors, and is indicated: in combination with other antiretroviral agents for the treatment of HIV-1 infection in adults and pediatric patients weighing at least 17 kg. HIV-1 PrEP ( 1.2 ): Emtricitabine and tenofovir disoproxil fumarate tablets are indicated in at-risk adults and adolescents weighing at least 35 kg for pre-exposure prophylaxis (PrEP) to reduce the risk of sexually acquired HIV-1 infection. Individuals must have a negative HIV-1 test immediately prior to…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59651-166

What is NDC 59651-166?
59651-166 is the product NDC for Emtricitabine and Tenofovir Disoproxil Fumarate, Emtricitabine 133 mg/1; Tenofovir disoproxil fumarate 200 mg/1 tablet, film coated, listed with the FDA by Aurobindo Pharma Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Emtricitabine and Tenofovir Disoproxil Fumarate.
What is the active ingredient?
Emtricitabine, Tenofovir disoproxil fumarate.
Who is the labeler?
Aurobindo Pharma Limited, NDC labeler code 59651. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Emtricitabine and Tenofovir Disoproxil Fumarate?
42 other product NDCs are listed under this name. See all 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 Emtricitabine and Tenofovir Disoproxil Fumarate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Emtricitabine and Tenofovir Disoproxil FumarateEmtricitabine 200 mg/1; Tenofovir disoproxil fumarate 300 mg/1Tablet, Film coatedOralAvKARE42291-98042291-0980-30
Emtricitabine and Tenofovir Disoproxil FumarateEmtricitabine 200 mg/1; Tenofovir disoproxil fumarate 300 mg/1Tablet, Film coatedOralQUALLENT PHARMACEUTICALS HEALTH LLC82009-10982009-0109-30
Emtricitabine and Tenofovir Disoproxil FumarateEmtricitabine 100 mg/1; Tenofovir disoproxil fumarate 150 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-16559651-0165-30
Emtricitabine and Tenofovir Disoproxil FumarateEmtricitabine 167 mg/1; Tenofovir disoproxil fumarate 250 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-16759651-0167-30
Emtricitabine and tenofovir disoproxil fumarateEmtricitabine 200 mg/1; Tenofovir disoproxil fumarate 300 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-802850090-8028-01
Emtricitabine and tenofovir disoproxil fumarateEmtricitabine 200 mg/1; Tenofovir disoproxil fumarate 300 mg/1Tablet, Film coatedOralNorthStar RxLLC16714-53416714-0534-01
Emtricitabine and tenofovir disoproxil fumarateEmtricitabine 200 mg/1; Tenofovir disoproxil fumarate 300 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-369568071-3695-03
Emtricitabine And Tenofovir Disoproxil FumarateEmtricitabine 200 mg/1; Tenofovir disoproxil fumarate 300 mg/1Tablet, Film coatedOralDirectRx72189-31272189-0312-03
Emtricitabine And Tenofovir Disoproxil FumarateEmtricitabine 200 mg/1; Tenofovir disoproxil fumarate 300 mg/1Tablet, Film coatedOralCipla USA Inc.69097-74169097-0741-02
Emtricitabine and tenofovir disoproxil fumarateEmtricitabine 200 mg/1; Tenofovir disoproxil fumarate 300 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-383168071-3831-03

All 43 Emtricitabine and Tenofovir Disoproxil Fumarate NDCs

Other NDCs under ANDA 211640

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

FDA NDC Directory listings under ANDA 211640
ProductStrengthForm · routeLabelerProduct NDC
Emtricitabine and Tenofovir Disoproxil FumarateEmtricitabine 100 mg/1; Tenofovir disoproxil fumarate 150 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-165
Emtricitabine and Tenofovir Disoproxil FumarateEmtricitabine 167 mg/1; Tenofovir disoproxil fumarate 250 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-167

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