Losartan Potassium and Hydrochlorothiazide NDC 0093-7369

NDC codes

FDA NDC Directory

Product NDC (as listed)0093-7369Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00093-7369Add 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 NDC	11-digit (billing)	Package
0093-7369-10	00093736910	1000 TABLET, FILM COATED in 1 BOTTLE (0093-7369-10)Marketed from Apr 6, 2010
0093-7369-56	00093736956	30 TABLET, FILM COATED in 1 BOTTLE (0093-7369-56)Marketed from Apr 6, 2010
0093-7369-98	00093736998	90 TABLET, FILM COATED in 1 BOTTLE (0093-7369-98)Marketed from Apr 6, 2010

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

Brand name (proprietary): Losartan Potassium and Hydrochlorothiazide
Generic name (nonproprietary): losartan potassium and hydrochlorothiazide
Active ingredients: Losartan potassium — 100 mg/1Hydrochlorothiazide — 12.5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Teva Pharmaceuticals USA, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077157
Marketing start: Apr 6, 2010
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers: Product ID 0093-7369_3fa33b06-383d-42a5-9349-35d3bdf9ab30SPL ID 3fa33b06-383d-42a5-9349-35d3bdf9ab30SPL set ID deafd195-7a1b-4ad8-a371-2cd9f433dea5RxCUI 979464, 979468, 979471UNII 0J48LPH2TH, 3ST302B24A
Pharmacologic class: Angiotensin 2 Receptor Blocker; Thiazide Diuretic

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

N400093736910 followed by a unit qualifier and the quantity

Package 00093-7369-10. 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

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