NDC codes

FDA NDC Directory
Product NDC (as listed)70010-187Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70010-0187Add 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
70010-187-03700100187037001001870330 TABLET, FILM COATED in 1 BOTTLE (70010-187-03)Marketed from Sep 29, 2023
70010-187-1070010018710700100187101000 TABLET, FILM COATED in 1 BOTTLE (70010-187-10)Marketed from Sep 29, 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)
losartan potassium and hydrochlorothiazide
Active ingredients
Losartan potassium — 50 mg/1Hydrochlorothiazide — 12.5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Granules Pharmaceuticals Inc.NDC labeler code 70010
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218015
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 70010-187_5d4eea9c-3657-5f79-e063-6294a90a58b7SPL ID 5d4eea9c-3657-5f79-e063-6294a90a58b7
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

N470010018703 followed by a unit qualifier and the quantity

Package 70010-0187-03. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70010-187

What is NDC 70010-187?
70010-187 is the product NDC for Losartan Potassium And Hydrochlorothiazide, Losartan potassium 50 mg/1; Hydrochlorothiazide 12.5 mg/1 tablet, film coated, listed with the FDA by Granules Pharmaceuticals Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Losartan Potassium And Hydrochlorothiazide.
What is the active ingredient?
Losartan potassium, Hydrochlorothiazide.
Who is the labeler?
Granules Pharmaceuticals Inc., NDC labeler code 70010. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Losartan Potassium And Hydrochlorothiazide?
107 other product NDCs are listed under this name. See all Losartan Potassium And Hydrochlorothiazide 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 Losartan Potassium And Hydrochlorothiazide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Losartan Potassium And HydrochlorothiazideLosartan potassium 50 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-75531722-0755-1031722-0755-3031722-0755-90
Losartan Potassium And HydrochlorothiazideLosartan potassium 100 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-75631722-0756-1031722-0756-3031722-0756-90
Losartan Potassium And HydrochlorothiazideLosartan potassium 100 mg/1; Hydrochlorothiazide 25 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-75731722-0757-1031722-0757-3031722-0757-90
Losartan Potassium and HydrochlorothiazideLosartan potassium 50 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralCoupler LLC67046-161867046-1618-03
Losartan potassium and HydrochlorothiazideLosartan potassium 100 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-249272162-2492-0072162-2492-09
Losartan Potassium and HydrochlorothiazideLosartan potassium 100 mg/1; Hydrochlorothiazide 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-782150090-7821-00
Losartan Potassium and HydrochlorothiazideLosartan potassium 100 mg/1; Hydrochlorothiazide 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-444750090-4447-0050090-4447-0150090-4447-02
Losartan Potassium and HydrochlorothiazideLosartan potassium 100 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralNorthStar Rx LLC16714-22416714-0224-0116714-0224-0216714-0224-03
Losartan Potassium and HydrochlorothiazideLosartan potassium 100 mg/1; Hydrochlorothiazide 25 mg/1Tablet, Film coatedOralNorthStar Rx LLC16714-22516714-0225-0116714-0225-0216714-0225-04
Losartan Potassium and HydrochlorothiazideLosartan potassium 50 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralNorthStar Rx LLC16714-22616714-0226-0116714-0226-0216714-0226-04

All 108 Losartan Potassium And Hydrochlorothiazide NDCs

Other NDCs under ANDA 218015

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

FDA NDC Directory listings under ANDA 218015
ProductStrengthForm · routeLabelerProduct NDC
Losartan Potassium And HydrochlorothiazideLosartan potassium 100 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralGranules Pharmaceuticals Inc.70010-188
Losartan Potassium And HydrochlorothiazideLosartan potassium 100 mg/1; Hydrochlorothiazide 25 mg/1Tablet, Film coatedOralGranules Pharmaceuticals Inc.70010-189

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