NDC codes

FDA NDC Directory
Product NDC (as listed)62332-409Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62332-0409Add 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
62332-409-306233204093030 CAPSULE in 1 BOTTLE (62332-409-30)Marketed from Aug 5, 2021
62332-409-3162332040931100 CAPSULE in 1 BOTTLE (62332-409-31)Marketed from Aug 5, 2021
62332-409-906233204099090 CAPSULE in 1 BOTTLE (62332-409-90)Marketed from Aug 5, 2021

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)
Clomipramine Hydrochloride
Generic name (nonproprietary)
clomipramine hydrochloride
Active ingredients
Clomipramine hydrochloride — 75 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211822
Marketing start
Listing expires
Identifiers
Product ID 62332-409_82f6f3ee-cfab-4483-9b7b-3dea57942cc2SPL ID 82f6f3ee-cfab-4483-9b7b-3dea57942cc2SPL set ID 73d14287-7aea-4971-b44d-6e1c9b575bb1RxCUI 857297, 857301, 857305UNII 2LXW0L6GWJUPC 0362332409303, 0362332407309
Pharmacologic class
Tricyclic Antidepressant

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

N462332040930 followed by a unit qualifier and the quantity

Package 62332-0409-30. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Clomipramine hydrochloride capsules are indicated for the treatment of obsessions and compulsions in patients with Obsessive-Compulsive Disorder (OCD). The obsessions or compulsions must cause marked distress, be time-consuming, or significantly interfere with social or occupational functioning, in order to meet the DSM-III-R (circa 1989) diagnosis of OCD. Obsessions are recurrent, persistent ideas, thoughts, images, or impulses that are ego­ dystonic. Compulsions are repetitive, purposeful, and intentional behaviors performed in response to an obsession or in a stereotyped fashion, and are recognized by the person as excessive or unreasonable. The effectiveness of clom…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 211822

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

FDA NDC Directory listings under ANDA 211822
ProductStrengthForm · routeLabelerProduct NDC
Clomipramine HydrochlorideClomipramine hydrochloride 25 mg/1CapsuleOralAlembic Pharmaceuticals Limited46708-407
Clomipramine HydrochlorideClomipramine hydrochloride 50 mg/1CapsuleOralAlembic Pharmaceuticals Limited46708-408
Clomipramine HydrochlorideClomipramine hydrochloride 75 mg/1CapsuleOralAlembic Pharmaceuticals Limited46708-409
Clomipramine HydrochlorideClomipramine hydrochloride 50 mg/1CapsuleOralAlembic Pharmaceuticals Inc.62332-408
Clomipramine HydrochlorideClomipramine hydrochloride 25 mg/1CapsuleOralAlembic Pharmaceuticals Inc.62332-407

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