What is NDC 70771-1529?

70771-1529 is the product NDC for doxepin, Doxepin hydrochloride 6 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 6 package NDCs, shown above in 10- and 11-digit form.

Zydus Lifesciences Limited, NDC labeler code 70771. 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?

23 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

doxepin NDC 70771-1529 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1529Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1529Add 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
70771-1529-0	7077115290070771152900	1000 TABLET in 1 BOTTLE (70771-1529-0)Marketed from Jun 30, 2024
70771-1529-1	7077115290170771152901	100 TABLET in 1 BOTTLE (70771-1529-1)Marketed from Jun 30, 2024
70771-1529-3	7077115290370771152903	30 TABLET in 1 BOTTLE (70771-1529-3)Marketed from Jun 30, 2024
70771-1529-4	7077115290470771152904	10 BLISTER PACK in 1 CARTON (70771-1529-4) / 10 TABLET in 1 BLISTER PACKMarketed from Jun 30, 2024
70771-1529-5	7077115290570771152905	500 TABLET in 1 BOTTLE (70771-1529-5)Marketed from Jun 30, 2024
70771-1529-9	7077115290970771152909	90 TABLET in 1 BOTTLE (70771-1529-9)Marketed from Jun 30, 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
Generic name (nonproprietary): doxepin
Active ingredients: Doxepin hydrochloride — 6 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202761
Marketing start: Jun 30, 2024
Listing expires: Dec 31, 2027
Identifiers: Product ID 70771-1529_2a2843b4-5867-4df6-af9a-dbe0264d6f1bSPL ID 2a2843b4-5867-4df6-af9a-dbe0264d6f1bSPL set ID 1461ede6-24f0-42a1-b801-0cf4ef404985RxCUI 966787, 966793UNII 3U9A0FE9N5UPC 0372578182069, 0372578181062
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

N470771152900 followed by a unit qualifier and the quantity

Package 70771-1529-00. 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

Current FDA label (SPL), effective Jan 8, 2025.

Full label on DailyMed (opens in a new tab)

About NDC 70771-1529

What is NDC 70771-1529?: 70771-1529 is the product NDC for doxepin, Doxepin hydrochloride 6 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: doxepin.
What is the active ingredient?: Doxepin hydrochloride.
Who is the labeler?: Zydus Lifesciences Limited, NDC labeler code 70771. 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?: 23 other product NDCs are listed under this name. See all doxepin 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 NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Doxepin	Doxepin hydrochloride 3 mg/1	TabletOral	NorthStar Rx LLC	72603-919	72603-0919-01
Doxepin	Doxepin hydrochloride 6 mg/1	TabletOral	NorthStar Rx LLC	72603-920	72603-0920-01
Doxepin	Doxepin hydrochloride 3 mg/1	TabletOral	Aurobindo Pharma Limited	59651-844	59651-0844-30
Doxepin	Doxepin hydrochloride 6 mg/1	TabletOral	Aurobindo Pharma Limited	59651-845	59651-0845-30
Doxepindoxepin hydrochloride	Doxepin hydrochloride 6 mg/1	TabletOral	REMEDYREPACK INC.	70518-4327	70518-4327-00
Doxepin	Doxepin hydrochloride 3 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-280	27241-0280-30
Doxepin	Doxepin hydrochloride 6 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-281	27241-0281-30
doxepin	Doxepin hydrochloride 3 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1528	70771-1528-0070771-1528-0170771-1528-03+3 more
doxepin	Doxepin hydrochloride 3 mg/1	TabletOral	Viona Pharmaceuticals Inc	72578-181	72578-0181-0172578-0181-0572578-0181-06+3 more
doxepin	Doxepin hydrochloride 6 mg/1	TabletOral	Viona Pharmaceuticals Inc	72578-182	72578-0182-0172578-0182-0572578-0182-06+3 more

All 24 doxepin NDCs

Other NDCs under ANDA 202761

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

FDA NDC Directory listings under ANDA 202761
Product	Strength	Form · route	Labeler	Product NDC
doxepin	Doxepin hydrochloride 3 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1528
doxepin	Doxepin hydrochloride 3 mg/1	TabletOral	Viona Pharmaceuticals Inc	72578-181
doxepin	Doxepin hydrochloride 6 mg/1	TabletOral	Viona Pharmaceuticals Inc	72578-182