NDC codes

FDA NDC Directory
Product NDC (as listed)71205-161Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0161Add 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
71205-161-07712050161077 CAPSULE in 1 BOTTLE, PLASTIC (71205-161-07)Marketed from May 1, 2019
71205-161-307120501613030 CAPSULE in 1 BOTTLE, PLASTIC (71205-161-30)Marketed from Nov 1, 2018
71205-161-607120501616060 CAPSULE in 1 BOTTLE, PLASTIC (71205-161-60)Marketed from Nov 1, 2018
71205-161-907120501619090 CAPSULE in 1 BOTTLE, PLASTIC (71205-161-90)Marketed from Nov 1, 2018

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

Brand name (proprietary)
hydrochlorothiazide
Generic name (nonproprietary)
hydrochlorothiazide
Active ingredients
Hydrochlorothiazide — 12.5 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090510
Marketing start
Listing expires
Other FDA classes
Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 71205-161_a58f29eb-fe30-469d-89db-eefea2703224SPL ID a58f29eb-fe30-469d-89db-eefea2703224SPL set ID 98edae8a-99dc-4f26-a956-3ad58bf38a26RxCUI 199903UNII 0J48LPH2THUPC 0371205161309
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

N471205016107 followed by a unit qualifier and the quantity

Package 71205-0161-07. 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 capsules are indicated in the management of hypertension either as the sole therapeutic agent, or in combination with other antihypertensives. Unlike potassium sparing combination diuretic products, hydrochlorothiazide capsules may be used in those patients in whom the development of hyperkalemia cannot be risked, including patients taking ACE inhibitors. Usage in Pregnancy : The routine use of diuretics in an otherwise healthy woman is inappropriate and exposes mother and fetus to unnecessary hazard. Diuretics do not prevent development of toxemia of pregnancy, and there is no satisfactory evidence that they are useful in the treatment of developed …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 090510

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

FDA NDC Directory listings under ANDA 090510
ProductStrengthForm · routeLabelerProduct NDC
hydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralQPharma Inc42708-086
hydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralNorthwind Health Company, LLC51655-522
hydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralUnichem Pharmaceuticals (USA), Inc.29300-130
hydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralA-S Medication Solutions50090-0724
hydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralAmerican Health Packaging60687-683
hydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralBryant Ranch Prepack71335-0067
hydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralQuality Care Products LLC35356-807

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