NDC codes

FDA NDC Directory
Product NDC (as listed)27241-290Labeler and product segments. Claims need a package NDC.
Product NDC at billing width27241-0290Add 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
27241-290-0127241029001100 CAPSULE in 1 BOTTLE (27241-290-01)Marketed from May 12, 2025
27241-290-10272410290101000 CAPSULE in 1 BOTTLE (27241-290-10)Marketed from May 12, 2025

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)
Terazosin
Generic name (nonproprietary)
terazosin
Active ingredients
Terazosin hydrochloride5 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 219482
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Antagonists (Mechanism)
Identifiers
Product ID 27241-290_ec1b00c3-3d59-420a-a71c-e9bd9a8d02fdSPL ID ec1b00c3-3d59-420a-a71c-e9bd9a8d02fdSPL set ID bed99c2a-4266-4a2c-bb0f-7643fdafff78RxCUI 260376, 313215, 313217, 313219UNII D32S14F082UPC 0327241289019, 0327241291012, 0327241290015, 0327241288012
Pharmacologic class
alpha-Adrenergic Blocker

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

N427241029001 followed by a unit qualifier and the quantity

Package 27241-0290-01. 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 Terazosin capsules are indicated for the treatment of symptomatic benign prostatic hyperplasia (BPH). There is a rapid response, with approximately 70% of patients experiencing an increase in urinary flow and improvement in symptoms of BPH when treated with terazosin capsules. The long-term effects of terazosin capsules on the incidence of surgery, acute urinary obstruction or other complications of BPH are yet to be determined. Terazosin capsules are also indicated for the treatment of hypertension. Terazosin capsules can be used alone or in combination with other antihypertensive agents such as diuretics or beta-adrenergic blocking agents.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 219482

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

FDA NDC Directory listings under ANDA 219482
ProductStrengthForm · routeLabelerProduct NDC
TerazosinTerazosin hydrochloride 10 mg/1CapsuleOralAjanta Pharma USA Inc.27241-291
TerazosinTerazosin hydrochloride 1 mg/1CapsuleOralAjanta Pharma USA Inc.27241-288
TerazosinTerazosin hydrochloride 2 mg/1CapsuleOralAjanta Pharma USA Inc.27241-289

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