NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1620Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1620Add 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
70771-1620-37077116200330 TABLET, FILM COATED in 1 BOTTLE (70771-1620-3)Marketed from Jul 1, 2021
70771-1620-47077116200410 BLISTER PACK in 1 CARTON (70771-1620-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1620-2)Marketed from Jul 1, 2021
70771-1620-97077116200990 TABLET, FILM COATED in 1 BOTTLE (70771-1620-9)Marketed from Jul 1, 2021

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)
Emtricitabine and tenofovir disoproxil fumarate
Generic name (nonproprietary)
emtricitabine and tenofovir disoproxil fumarate
Active ingredients
Emtricitabine — 100 mg/1Tenofovir disoproxil fumarate — 150 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212689
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 70771-1620_8fb1b15c-e324-4410-9a1b-2b3a2ffee3f6SPL ID 8fb1b15c-e324-4410-9a1b-2b3a2ffee3f6SPL set ID a0ee89b6-72c3-4b99-8d1c-d7473f1d5ef3RxCUI 476556, 1744001, 1744005, 1744009UNII OTT9J7900I, G70B4ETF4S
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

N470771162003 followed by a unit qualifier and the quantity

Package 70771-1620-03. 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 .

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 212689

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

FDA NDC Directory listings under ANDA 212689
ProductStrengthForm · routeLabelerProduct NDC
Emtricitabine and tenofovir disoproxil fumarateEmtricitabine 133 mg/1; Tenofovir disoproxil fumarate 200 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1621
Emtricitabine and tenofovir disoproxil fumarateEmtricitabine 167 mg/1; Tenofovir disoproxil fumarate 250 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1622
Emtricitabine and tenofovir disoproxil fumarateEmtricitabine 200 mg/1; Tenofovir disoproxil fumarate 300 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1709
Emtricitabine and tenofovir disoproxil fumarateEmtricitabine 200 mg/1; Tenofovir disoproxil fumarate 300 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-1367
Emtricitabine and tenofovir disoproxil fumarateEmtricitabine 100 mg/1; Tenofovir disoproxil fumarate 150 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-1364
Emtricitabine and tenofovir disoproxil fumarateEmtricitabine 133 mg/1; Tenofovir disoproxil fumarate 200 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-1365
Emtricitabine and tenofovir disoproxil fumarateEmtricitabine 167 mg/1; Tenofovir disoproxil fumarate 250 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-1366

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