NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4238Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4238Add 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
70518-4238-07051842380030 CAPSULE in 1 BLISTER PACK (70518-4238-0)Marketed from Dec 13, 2024

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)
Doxepin Hydrochloride
Generic name (nonproprietary)
doxepin hydrochloride
Active ingredients
Doxepin hydrochloride — 25 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215113
Marketing start
Listing expires
Identifiers
Product ID 70518-4238_5a6de351-3a3f-1095-e063-6294a90a52ffSPL ID 5a6de351-3a3f-1095-e063-6294a90a52ffSPL set ID d29a8c70-cf1c-4bf8-bb87-1c80babce64eRxCUI 1000070UNII 3U9A0FE9N5
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

N470518423800 followed by a unit qualifier and the quantity

Package 70518-4238-00. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 215113

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

FDA NDC Directory listings under ANDA 215113
ProductStrengthForm · routeLabelerProduct NDC
Doxepin HydrochlorideDoxepin hydrochloride 50 mg/1CapsuleOralBryant Ranch Prepack71335-2804
Doxepin HydrochlorideDoxepin hydrochloride 100 mg/1CapsuleOralREMEDYREPACK INC.70518-4179
Doxepin HCLDoxepin hydrochloride 10 mg/1CapsuleOralDirect_Rx72189-633
Doxepin HydrochlorideDoxepin hydrochloride 75 mg/1CapsuleOralREMEDYREPACK INC.70518-4222
Doxepin HydrochlorideDoxepin hydrochloride 50 mg/1CapsuleOralREMEDYREPACK INC.70518-4231
Doxepin HydrochlorideDoxepin hydrochloride 10 mg/1CapsuleOralREMEDYREPACK INC.70518-4252
Doxepin HydrochlorideDoxepin hydrochloride 25 mg/1CapsuleOralBryant Ranch Prepack71335-2418
Doxepin HydrochlorideDoxepin hydrochloride 10 mg/1CapsuleOralBryant Ranch Prepack71335-2452
Doxepin HydrochlorideDoxepin hydrochloride 10 mg/1CapsuleOralProficient Rx LP82804-305
Doxepin HydrochlorideDoxepin hydrochloride 50 mg/1CapsuleOralNovadoz Pharmaceuticals LLC72205-090
Doxepin HydrochlorideDoxepin hydrochloride 10 mg/1CapsuleOralNovadoz Pharmaceuticals LLC72205-088
Doxepin HydrochlorideDoxepin hydrochloride 25 mg/1CapsuleOralNovadoz Pharmaceuticals LLC72205-089
Doxepin HydrochlorideDoxepin hydrochloride 75 mg/1CapsuleOralNovadoz Pharmaceuticals LLC72205-091
Doxepin HydrochlorideDoxepin hydrochloride 100 mg/1CapsuleOralNovadoz Pharmaceuticals LLC72205-092
Doxepin HydrochlorideDoxepin hydrochloride 50 mg/1CapsuleOralA-S Medication Solutions50090-7819

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