NDC codes

FDA NDC Directory
Product NDC (as listed)59651-176Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59651-0176Add 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
59651-176-0159651017601100 CAPSULE in 1 BOTTLE (59651-176-01)Marketed from Mar 27, 2019

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)
Doxepin Hydrochloride
Generic name (nonproprietary)
doxepin hydrochloride
Active ingredients
Doxepin hydrochloride — 75 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211603
Marketing start
Listing expires
Identifiers
Product ID 59651-176_5b5efe70-cce2-4950-94f0-d3aa869e442eSPL ID 5b5efe70-cce2-4950-94f0-d3aa869e442eSPL set ID f3c242dd-426e-4c69-8f21-2645361d5f27RxCUI 1000048, 1000058, 1000070, 1000076, 1000097UNII 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

N459651017601 followed by a unit qualifier and the quantity

Package 59651-0176-01. 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)

Doxepin hydrochloride capsules are indicated for the treatment of major depressive disorder (MDD) in adults. Doxepin hydrochloride capsules are a tricyclic antidepressant (TCA) indicated for the treatment of major depressive disorder (MDD) in adults ( 1 ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 211603

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

FDA NDC Directory listings under ANDA 211603
ProductStrengthForm · routeLabelerProduct NDC
Doxepin HydrochlorideDoxepin hydrochloride 10 mg/1CapsuleOralProficient Rx LP71205-534
Doxepin HydrochlorideDoxepin hydrochloride 10 mg/1CapsuleOralPD-Rx Pharmaceuticals, Inc.72789-220
Doxepin HydrochlorideDoxepin hydrochloride 25 mg/1CapsuleOralProficient Rx LP71205-610
Doxepin HydrochlorideDoxepin hydrochloride 25 mg/1CapsuleOralPD-Rx Pharmaceuticals, Inc.72789-542
Doxepin HydrochlorideDoxepin hydrochloride 10 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-5179
Doxepin HydrochlorideDoxepin hydrochloride 50 mg/1CapsuleOralAurobindo Pharma Limited59651-175
Doxepin HydrochlorideDoxepin hydrochloride 10 mg/1CapsuleOralAurobindo Pharma Limited59651-173
Doxepin HydrochlorideDoxepin hydrochloride 25 mg/1CapsuleOralAurobindo Pharma Limited59651-174
Doxepin HydrochlorideDoxepin hydrochloride 100 mg/1CapsuleOralAurobindo Pharma Limited59651-177

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Doxepin Hydrochloride NDC 59651-176 | Med-Code