Prescription drug · ANDA

Desipramine Hydrochloride NDC 50742-116

Desipramine hydrochloride 100 mg/1 · Tablet · Oral · Ingenus Pharmaceuticals, LLC

NDC codes

FDA NDC Directory
Product NDC (as listed)50742-116Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50742-0116Add 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
50742-116-0150742011601100 TABLET in 1 BOTTLE (50742-116-01)Marketed from Sep 19, 2018

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 — 100 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204963
Marketing start
Listing expires
Identifiers
Product ID 50742-116_7a0e5dd9-7456-4774-b529-ce9d5627b654SPL ID 7a0e5dd9-7456-4774-b529-ce9d5627b654SPL set ID 7280f157-3fff-41c5-b3f4-510b8bacdabaRxCUI 1099288, 1099292, 1099296, 1099300, 1099304, 1099316UNII 1Y58DO4MY1UPC 0350742112012, 0350742116010, 0350742114016, 0350742117505, 0350742113019, 0350742115013
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

N450742011601 followed by a unit qualifier and the quantity

Package 50742-0116-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Desipramine hydrochloride tablets is 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 204963

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

FDA NDC Directory listings under ANDA 204963
ProductStrengthForm · routeLabelerProduct NDC
Desipramine HCLDesipramine hydrochloride 10 mg/1TabletOralDirect_Rx72189-391
Desipramine HydrochlorideDesipramine hydrochloride 10 mg/1TabletOralREMEDYREPACK INC.70518-4645
Desipramine HydrochlorideDesipramine hydrochloride 10 mg/1TabletOralIngenus Pharmaceuticals, LLC50742-112
Desipramine HydrochlorideDesipramine hydrochloride 25 mg/1TabletOralIngenus Pharmaceuticals, LLC50742-113
Desipramine HydrochlorideDesipramine hydrochloride 150 mg/1TabletOralIngenus Pharmaceuticals, LLC50742-117
Desipramine HydrochlorideDesipramine hydrochloride 50 mg/1TabletOralIngenus Pharmaceuticals, LLC50742-114
Desipramine HydrochlorideDesipramine hydrochloride 75 mg/1TabletOralIngenus Pharmaceuticals, LLC50742-115

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Desipramine Hydrochloride NDC 50742-116 | Med-Code