NDC codes

FDA NDC Directory
Product NDC (as listed)70518-3208Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-3208Add 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
70518-3208-07051832080090 TABLET in 1 BOTTLE (70518-3208-0)Marketed from Aug 7, 2022

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)
Levothyroxine sodium
Generic name (nonproprietary)
levothyroxine sodium
Active ingredients
Levothyroxine sodium — 50 ug/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212399
Marketing start
Listing expires
Other FDA classes
Thyroxine (Chemical structure)
Identifiers
Product ID 70518-3208_4ece584d-5b9b-6e34-e063-6394a90a307aSPL ID 4ece584d-5b9b-6e34-e063-6394a90a307aSPL set ID c7d5b71b-e983-4b1a-bfc2-d2343cf8668cRxCUI 966221UNII 9J765S329G
Pharmacologic class
l-Thyroxine

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

N470518320800 followed by a unit qualifier and the quantity

Package 70518-3208-00. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 212399

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

FDA NDC Directory listings under ANDA 212399
ProductStrengthForm · routeLabelerProduct NDC
Levothyroxine sodiumLevothyroxine sodium 50 ug/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-272
Levothyroxine sodiumLevothyroxine sodium 100 ug/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-297
Levothyroxine sodiumLevothyroxine sodium 200 ug/1TabletOralBryant Ranch Prepack71335-2090
Levothyroxine sodiumLevothyroxine sodium 200 ug/1TabletOralNuCare Pharmaceuticals,Inc.68071-3619
Levothyroxine sodiumLevothyroxine sodium 88 ug/1TabletOralREMEDYREPACK INC.70518-3154
Levothyroxine sodiumLevothyroxine sodium 50 ug/1TabletOralProficient Rx LP71205-646
Levothyroxine sodiumLevothyroxine sodium 25 ug/1TabletOralProficient Rx LP82804-168
Levothyroxine sodiumLevothyroxine sodium 100 ug/1TabletOralBryant Ranch Prepack71335-2138
Levothyroxine sodiumLevothyroxine sodium 137 ug/1TabletOralBryant Ranch Prepack71335-1861
Levothyroxine sodiumLevothyroxine sodium 50 ug/1TabletOralAccord Healthcare Inc.16729-448
Levothyroxine sodiumLevothyroxine sodium 25 ug/1TabletOralAccord Healthcare Inc.16729-447
Levothyroxine sodiumLevothyroxine sodium 112 ug/1TabletOralAccord Healthcare Inc.16729-452
Levothyroxine sodiumLevothyroxine sodium 25 ug/1TabletOralBryant Ranch Prepack71335-1881
Levothyroxine sodiumLevothyroxine sodium 75 ug/1TabletOralAccord Healthcare Inc.16729-449
Levothyroxine sodiumLevothyroxine sodium 88 ug/1TabletOralAccord Healthcare Inc.16729-450
Levothyroxine sodiumLevothyroxine sodium 75 ug/1TabletOralREMEDYREPACK INC.70518-3274
Levothyroxine sodiumLevothyroxine sodium 100 ug/1TabletOralAccord Healthcare Inc.16729-451
Levothyroxine sodiumLevothyroxine sodium 150 ug/1TabletOralAccord Healthcare Inc.16729-455
Levothyroxine sodiumLevothyroxine sodium 125 ug/1TabletOralProficient Rx LP71205-681
Levothyroxine sodiumLevothyroxine sodium 125 ug/1TabletOralAccord Healthcare Inc.16729-453

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