NDC codes

FDA NDC Directory
Product NDC (as listed)70954-365Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70954-0365Add 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
70954-365-1070954036510100 CAPSULE in 1 BOTTLE (70954-365-10)Marketed from Jul 19, 2022

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)
Phenoxybenzamine Hydrochloride
Generic name (nonproprietary)
phenoxybenzamine hydrochloride
Active ingredients
Phenoxybenzamine hydrochloride — 10 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Novitium Pharma LLCNDC labeler code 70954
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215042
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Antagonists (Mechanism)
Identifiers
Product ID 70954-365_235c3c98-4dc2-4b5e-8bdc-f21d18cbb7acSPL ID 235c3c98-4dc2-4b5e-8bdc-f21d18cbb7acSPL set ID 2cb5fcd7-c37f-41de-8beb-0c7eded9ed04RxCUI 861402UNII X1IEG24OHLUPC 0370954365105
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

N470954036510 followed by a unit qualifier and the quantity

Package 70954-0365-10. 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 & 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 70954-365

What is NDC 70954-365?
70954-365 is the product NDC for Phenoxybenzamine Hydrochloride, Phenoxybenzamine hydrochloride 10 mg/1 capsule, listed with the FDA by Novitium Pharma 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?
Novitium Pharma LLC, NDC labeler code 70954. 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/1CapsuleOralAurobindo Pharma Limited59651-32759651-0327-01
Phenoxybenzamine HydrochloridePhenoxybenzamine hydrochloride 10 mg/1CapsuleOralBurel Pharmaceuticals, LLC35573-47335573-0473-02
Phenoxybenzamine hydrochloridePhenoxybenzamine hydrochloride 10 mg/1CapsuleOralAmneal Pharmaceuticals NY LLC60219-150260219-1502-01

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