NDC codes

FDA NDC Directory
Product NDC (as listed)72789-492Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72789-0492Add 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
72789-492-017278904920172789049201100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-492-01)Marketed from Mar 10, 2025
72789-492-9572789049295727890492951000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-492-95)Marketed from Mar 10, 2025

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)
Imipramine Hydrochloride
Generic name (nonproprietary)
imipramine hydrochloride
Active ingredients
Imipramine hydrochloride — 25 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
PD-Rx Pharmaceuticals, Inc.NDC labeler code 72789
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040903
Marketing start
Listing expires
Identifiers
Product ID 72789-492_5b8b76f8-b753-3aa4-e063-6294a90a9541SPL ID 5b8b76f8-b753-3aa4-e063-6294a90a9541
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

N472789049201 followed by a unit qualifier and the quantity

Package 72789-0492-01. 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.

About NDC 72789-492

What is NDC 72789-492?
72789-492 is the product NDC for Imipramine Hydrochloride, Imipramine hydrochloride 25 mg/1 tablet, film coated, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Imipramine Hydrochloride.
What is the active ingredient?
Imipramine hydrochloride.
Who is the labeler?
PD-Rx Pharmaceuticals, Inc., NDC labeler code 72789. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Imipramine Hydrochloride?
30 other product NDCs are listed under this name. See all Imipramine 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 Imipramine Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Imipramine HydrochlorideImipramine hydrochloride 25 mg/1Tablet, Film coatedOralCoupler LLC67046-156467046-1564-03
Imipramine HydrochlorideImipramine hydrochloride 25 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-034280425-0342-0180425-0342-0280425-0342-03
Imipramine hydrochlorideImipramine hydrochloride 10 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-029480425-0294-0180425-0294-0280425-0294-03
Imipramine HydrochlorideImipramine hydrochloride 25 mg/1Tablet, Film coatedOralKey Therapeutics70868-81070868-0810-10
Imipramine HydrochlorideImipramine hydrochloride 25 mg/1TabletOralStrides Pharma Science Limited64380-17064380-0170-0164380-0170-02
Imipramine HydrochlorideImipramine hydrochloride 10 mg/1TabletOralStrides Pharma Science Limited64380-16964380-0169-0164380-0169-02
Imipramine HydrochlorideImipramine hydrochloride 50 mg/1TabletOralStrides Pharma Science Limited64380-17164380-0171-0164380-0171-02
Imipramine HydrochlorideImipramine hydrochloride 25 mg/1TabletOralREMEDYREPACK INC.70518-352670518-3526-0070518-3526-0170518-3526-03
Imipramine HydrochlorideImipramine hydrochloride 50 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-366968071-3669-09
Imipramine HydrochlorideImipramine hydrochloride 10 mg/1TabletOralOxford Pharmaceuticals, LLC69584-42569584-0425-1069584-0425-90

All 31 Imipramine Hydrochloride NDCs

Other NDCs under ANDA 040903

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

FDA NDC Directory listings under ANDA 040903
ProductStrengthForm · routeLabelerProduct NDC
Imipramine HydrochlorideImipramine hydrochloride 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-3148
Imipramine HydrochlorideImipramine hydrochloride 25 mg/1Tablet, Film coatedOralCoupler LLC67046-1564
Imipramine HydrochlorideImipramine hydrochloride 10 mg/1Tablet, Film coatedOralLeading Pharma, LLC69315-133
Imipramine HydrochlorideImipramine hydrochloride 25 mg/1Tablet, Film coatedOralLeading Pharma, LLC69315-134
Imipramine HydrochlorideImipramine hydrochloride 50 mg/1Tablet, Film coatedOralLeading Pharma, LLC69315-135
Imipramine HydrochlorideImipramine hydrochloride 50 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-1588
Imipramine HydrochlorideImipramine hydrochloride 10 mg/1Tablet, Film coatedOralProficient Rx LP71205-804
Imipramine HydrochlorideImipramine hydrochloride 25 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2601
Imipramine HydrochlorideImipramine hydrochloride 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-3106
Imipramine HydrochlorideImipramine hydrochloride 50 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-493
Imipramine hydrochlorideImipramine hydrochloride 10 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0294

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