NDC codes

FDA NDC Directory
Product NDC (as listed)62332-318Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62332-0318Add 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
62332-318-306233203183030 TABLET, FILM COATED in 1 BOTTLE (62332-318-30)Marketed from Jul 8, 2021
62332-318-3162332031831100 TABLET, FILM COATED in 1 BOTTLE (62332-318-31)Marketed from Jul 8, 2021
62332-318-91623320318911000 TABLET, FILM COATED in 1 BOTTLE (62332-318-91)Marketed from Jul 8, 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)
Desipramine Hydrochloride
Generic name (nonproprietary)
desipramine hydrochloride
Active ingredients
Desipramine hydrochloride — 75 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209785
Marketing start
Listing expires
Identifiers
Product ID 62332-318_06c52509-29c8-41c5-8492-3458df75f3d5SPL ID 06c52509-29c8-41c5-8492-3458df75f3d5SPL set ID cad14805-64d8-4257-b5f1-d56e0063f0e2RxCUI 1099288, 1099292, 1099296, 1099300, 1099304, 1099316UNII 1Y58DO4MY1UPC 0362332320318
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

N462332031830 followed by a unit qualifier and the quantity

Package 62332-0318-30. 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 Desipramine hydrochloride tablets, USP are indicated for the treatment of depression.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 209785

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

FDA NDC Directory listings under ANDA 209785
ProductStrengthForm · routeLabelerProduct NDC
Desipramine HydrochlorideDesipramine hydrochloride 25 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-316
Desipramine HydrochlorideDesipramine hydrochloride 10 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-315
Desipramine HydrochlorideDesipramine hydrochloride 150 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-320
Desipramine HydrochlorideDesipramine hydrochloride 50 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-317
Desipramine HydrochlorideDesipramine hydrochloride 75 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-318
Desipramine HydrochlorideDesipramine hydrochloride 100 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-319
Desipramine HydrochlorideDesipramine hydrochloride 50 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Inc.62332-317
Desipramine HydrochlorideDesipramine hydrochloride 10 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Inc.62332-315
Desipramine HydrochlorideDesipramine hydrochloride 25 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Inc.62332-316
Desipramine HydrochlorideDesipramine hydrochloride 100 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Inc.62332-319
Desipramine HydrochlorideDesipramine hydrochloride 150 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Inc.62332-320

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