Prescription drug · ANDA

Desipramine Hydrochloride (desipramine) NDC 69238-1059

Desipramine hydrochloride 75 mg/1 · Tablet, Film coated · Oral · Amneal Pharmaceuticals LLC

NDC codes

FDA NDC Directory
Product NDC (as listed)69238-1059Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69238-1059Add 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
69238-1059-169238105901100 TABLET, FILM COATED in 1 BOTTLE (69238-1059-1)Marketed from Mar 21, 2016
69238-1059-36923810590330 TABLET, FILM COATED in 1 BOTTLE (69238-1059-3)Marketed from Mar 21, 2016

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)
Desipramine Hydrochloride
Generic name (nonproprietary)
desipramine
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 208105
Marketing start
Marketing end
Identifiers
Product ID 69238-1059_6ea5e8b8-b492-440b-9e38-4ef1c0b46ee2SPL ID 6ea5e8b8-b492-440b-9e38-4ef1c0b46ee2
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

N469238105901 followed by a unit qualifier and the quantity

Package 69238-1059-01. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 208105

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

FDA NDC Directory listings under ANDA 208105
ProductStrengthForm · routeLabelerProduct NDC
Desipramine HydrochloridedesipramineDesipramine hydrochloride 100 mg/1Tablet, Film coatedOralAmneal Pharmaceuticals LLC69238-1061
Desipramine HydrochloridedesipramineDesipramine hydrochloride 10 mg/1Tablet, Film coatedOralAmneal Pharmaceuticals LLC69238-1053
Desipramine HydrochloridedesipramineDesipramine hydrochloride 25 mg/1Tablet, Film coatedOralAmneal Pharmaceuticals LLC69238-1055
Desipramine HydrochloridedesipramineDesipramine hydrochloride 50 mg/1Tablet, Film coatedOralAmneal Pharmaceuticals LLC69238-1057
Desipramine HydrochloridedesipramineDesipramine hydrochloride 150 mg/1Tablet, Film coatedOralAmneal Pharmaceuticals LLC69238-1063

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Desipramine Hydrochloride (desipramine) NDC 69238-1059 | Med-Code