NDC codes

FDA NDC Directory
Product NDC (as listed)60219-1502Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60219-1502Add 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
60219-1502-160219150201100 CAPSULE in 1 BOTTLE (60219-1502-1)Marketed from Oct 30, 2020

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)
Phenoxybenzamine hydrochloride
Generic name (nonproprietary)
phenoxybenzamine hydrochloride
Active ingredients
Phenoxybenzamine hydrochloride — 10 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Amneal Pharmaceuticals NY LLCNDC labeler code 60219
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212568
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Antagonists (Mechanism)
Identifiers
Product ID 60219-1502_7e30ff83-c617-4830-b75e-1897242c3a1aSPL ID 7e30ff83-c617-4830-b75e-1897242c3a1aSPL set ID 0be6a394-cd10-42fc-97cf-ad53d81d8d93RxCUI 861402UNII X1IEG24OHL
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

N460219150201 followed by a unit qualifier and the quantity

Package 60219-1502-01. 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)

INDICATION AND USAGE Phenoxybenzamine hydrochloride capsules are indicated in the treatment of pheochromocytoma, to control episodes of hypertension and sweating. If tachycardia is excessive, it may be necessary to use a beta -blocking agent concomitantly.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60219-1502

What is NDC 60219-1502?
60219-1502 is the product NDC for Phenoxybenzamine hydrochloride, Phenoxybenzamine hydrochloride 10 mg/1 capsule, listed with the FDA by Amneal Pharmaceuticals NY LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Phenoxybenzamine hydrochloride.
What is the active ingredient?
Phenoxybenzamine hydrochloride.
Who is the labeler?
Amneal Pharmaceuticals NY LLC, NDC labeler code 60219. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Phenoxybenzamine hydrochloride?
4 other product NDCs are listed under this name. See all Phenoxybenzamine hydrochloride 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 Phenoxybenzamine hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
phenoxybenzamine hydrochloridePhenoxybenzamine hydrochloride 10 mg/1CapsuleOralRising Pharma Holdings, Inc.16571-87416571-0874-01
Phenoxybenzamine HydrochloridePhenoxybenzamine hydrochloride 10 mg/1CapsuleOralBurel Pharmaceuticals, LLC35573-47335573-0473-02
Phenoxybenzamine HydrochloridePhenoxybenzamine hydrochloride 10 mg/1CapsuleOralAurobindo Pharma Limited59651-32759651-0327-01
Phenoxybenzamine HydrochloridePhenoxybenzamine hydrochloride 10 mg/1CapsuleOralNovitium Pharma LLC70954-36570954-0365-10

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