NDC codes

FDA NDC Directory
Product NDC (as listed)50090-6157Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-6157Add 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
50090-6157-05009061570030 TABLET in 1 BOTTLE (50090-6157-0)Marketed from Oct 7, 2022
50090-6157-150090615701100 TABLET in 1 BOTTLE (50090-6157-1)Marketed from Oct 7, 2022
50090-6157-850090615708200 TABLET in 1 BOTTLE (50090-6157-8)Marketed from Oct 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)
Hydrochlorothiazide
Generic name (nonproprietary)
hydrochlorothiazide
Active ingredients
Hydrochlorothiazide — 25 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 087059
Marketing start
Listing expires
Other FDA classes
Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 50090-6157_06b5df0b-d602-4e3b-b2aa-43df95f41196SPL ID 06b5df0b-d602-4e3b-b2aa-43df95f41196SPL set ID 1bb00980-eeea-4722-b010-e208f3ec2214RxCUI 310798UNII 0J48LPH2TH
Pharmacologic class
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

N450090615700 followed by a unit qualifier and the quantity

Package 50090-6157-00. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE Hydrochlorothiazide tablets are indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. Hydrochlorothiazide has also been found useful in edema due to various forms of renal dysfunction such as the nephrotic syndrome, acute glomerulonephritis, and chronic renal failure. Hydrochlorothiazide is indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effectiveness of other antihypertensive drugs in the more severe forms of hypertension.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 087059

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

FDA NDC Directory listings under ANDA 087059
ProductStrengthForm · routeLabelerProduct NDC
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralProficient Rx LP82804-972
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-296
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralNorthwind Health Company, LLC51655-088
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralOxford Pharmaceuticals, LLC69584-361
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-381
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralA-S Medication Solutions50090-6158
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralA-S Medication Solutions50090-6160
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralREMEDYREPACK INC.70518-4113

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