What is NDC 71335-9732?

71335-9732 is the product NDC for Doxepin hydrochloride, Doxepin hydrochloride 50 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 4 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Doxepin hydrochloride?

173 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Doxepin hydrochloride NDC 71335-9732

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-9732Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-9732Add 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 NDC	11-digit (billing)	Package
71335-9732-1	7133597320171335973201	60 CAPSULE in 1 BOTTLE (71335-9732-1)Marketed from Jun 30, 2023
71335-9732-2	7133597320271335973202	30 CAPSULE in 1 BOTTLE (71335-9732-2)Marketed from Jun 30, 2023
71335-9732-3	7133597320371335973203	90 CAPSULE in 1 BOTTLE (71335-9732-3)Marketed from Jun 30, 2023
71335-9732-4	7133597320471335973204	120 CAPSULE in 1 BOTTLE (71335-9732-4)Marketed from Jun 30, 2023

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 — 50 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212624
Marketing start: Dec 20, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 71335-9732_cfc63853-77b0-4c21-981e-ddea13fcc09cSPL ID cfc63853-77b0-4c21-981e-ddea13fcc09cSPL set ID 41046d94-1443-4bbd-96d0-8463604ae459RxCUI 1000076UNII 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

N471335973201 followed by a unit qualifier and the quantity

Package 71335-9732-01. 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 Jun 30, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Doxepin Hydrochloride Capsules, USP are recommended for the treatment of: Psychoneurotic patients with depression and/or anxiety. Depression and/or anxiety associated with alcoholism (not to be taken concomitantly with alcohol). Depression and/or anxiety associated with organic disease (the possibility of drug interaction should be considered if the patient is receiving other drugs concomitantly). Psychotic depressive disorders with associated anxiety including involutional depression and manic-depressive disorders. The target symptoms of psychoneurosis that respond particularly well to doxepin hydrochloride capsules include anxiety, tension, depression, somatic symptom…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-9732

What is NDC 71335-9732?: 71335-9732 is the product NDC for Doxepin hydrochloride, Doxepin hydrochloride 50 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Doxepin hydrochloride.
What is the active ingredient?: Doxepin hydrochloride.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Doxepin hydrochloride?: 173 other product NDCs are listed under this name. See all Doxepin 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 Doxepin hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Doxepin Hydrochloride	Doxepin hydrochloride 50 mg/g	CreamTopical	Sun Pharmaceutical Industries, Inc.	51672-1404	51672-1404-0251672-1404-09
Doxepin Hydrochloride	Doxepin hydrochloride 150 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4733	70518-4733-00
Doxepin hydrochloride	Doxepin hydrochloride 50 mg/1	CapsuleOral	Coupler LLC	67046-0394	67046-0394-03
Doxepin hydrochloride	Doxepin hydrochloride 25 mg/1	CapsuleOral	Coupler LLC	67046-0393	67046-0393-03
Doxepin Hydrochloride	Doxepin hydrochloride 10 mg/1	CapsuleOral	Safecor Health, LLC	48433-035	48433-0035-20
Doxepin Hydrochloride	Doxepin hydrochloride 25 mg/1	CapsuleOral	Safecor Health, LLC	48433-036	48433-0036-20
Doxepin Hydrochloride	Doxepin hydrochloride 50 mg/1	CapsuleOral	Safecor Health, LLC	48433-037	48433-0037-20
Doxepin Hydrochloride	Doxepin hydrochloride 100 mg/1	CapsuleOral	Safecor Health, LLC	48433-038	48433-0038-20
doxepin hydrochloride	Doxepin hydrochloride 3 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	51672-4246	51672-4246-02
doxepin hydrochloride	Doxepin hydrochloride 6 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	51672-4247	51672-4247-02

All 174 Doxepin hydrochloride NDCs

Other NDCs under ANDA 212624

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

FDA NDC Directory listings under ANDA 212624
Product	Strength	Form · route	Labeler	Product NDC
Doxepin hydrochloride	Doxepin hydrochloride 10 mg/1	CapsuleOral	Proficient Rx LP	71205-695
Doxepin hydrochloride	Doxepin hydrochloride 10 mg/1	CapsuleOral	Ajanta Pharma USA Inc.	27241-167
Doxepin hydrochloride	Doxepin hydrochloride 25 mg/1	CapsuleOral	Ajanta Pharma USA Inc.	27241-168
Doxepin hydrochloride	Doxepin hydrochloride 50 mg/1	CapsuleOral	Ajanta Pharma USA Inc.	27241-169
Doxepin hydrochloride	Doxepin hydrochloride 75 mg/1	CapsuleOral	Ajanta Pharma USA Inc.	27241-170
Doxepin hydrochloride	Doxepin hydrochloride 100 mg/1	CapsuleOral	Ajanta Pharma USA Inc.	27241-171
Doxepin hydrochloride	Doxepin hydrochloride 25 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-2188
Doxepin hydrochloride	Doxepin hydrochloride 10 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-3594
Doxepin hydrochloride	Doxepin hydrochloride 25 mg/1	CapsuleOral	Proficient Rx LP	82804-011
Doxepin HCL	Doxepin hydrochloride 25 mg/1	CapsuleOral	Direct_Rx	72189-533
Doxepin hydrochloride	Doxepin hydrochloride 50 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-3767
Doxepin hydrochloride	Doxepin hydrochloride 25 mg/1	CapsuleOral	Coupler LLC	67046-0393
Doxepin hydrochloride	Doxepin hydrochloride 50 mg/1	CapsuleOral	Coupler LLC	67046-0394
Doxepin hydrochloride	Doxepin hydrochloride 10 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-2092