What is NDC 70756-203?

70756-203 is the product NDC for Amitriptyline Hydrochloride, Amitriptyline hydrochloride 50 mg/1 tablet, film coated, listed with the FDA by Lifestar Pharma LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Lifestar Pharma LLC, NDC labeler code 70756. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Amitriptyline Hydrochloride?

200 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Amitriptyline Hydrochloride NDC 70756-203

NDC codes

FDA NDC Directory

Product NDC (as listed)70756-203Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70756-0203Add 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	Copy
70756-203-11	70756020311	100 TABLET, FILM COATED in 1 BOTTLE (70756-203-11)Marketed from Feb 23, 2021
70756-203-12	70756020312	1000 TABLET, FILM COATED in 1 BOTTLE (70756-203-12)Marketed from Feb 23, 2021

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): Amitriptyline Hydrochloride
Generic name (nonproprietary): amitriptyline hydrochloride
Active ingredients: Amitriptyline hydrochloride — 50 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Lifestar Pharma LLCNDC labeler code 70756
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213999
Marketing start: Feb 23, 2021
Listing expires: Dec 31, 2027
Identifiers: Product ID 70756-203_2595d2ab-fd5d-462c-82d4-656d20aa9415SPL ID 2595d2ab-fd5d-462c-82d4-656d20aa9415SPL set ID 67e31675-1da2-4acf-84ac-77522b02f0b9RxCUI 856762, 856773, 856783, 856834, 856845, 856853UNII 26LUD4JO9KUPC 0370756203124, 0370756206118
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

N470756020311 followed by a unit qualifier and the quantity

Package 70756-0203-11. 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 Apr 8, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE For the relief of symptoms of depression. Endogenous depression is more likely to be alleviated than are other depressive states.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70756-203

What is NDC 70756-203?: 70756-203 is the product NDC for Amitriptyline Hydrochloride, Amitriptyline hydrochloride 50 mg/1 tablet, film coated, listed with the FDA by Lifestar Pharma LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Amitriptyline Hydrochloride.
What is the active ingredient?: Amitriptyline hydrochloride.
Who is the labeler?: Lifestar Pharma LLC, NDC labeler code 70756. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Amitriptyline Hydrochloride?: 200 other product NDCs are listed under this name. See all Amitriptyline 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 Amitriptyline Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 25 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0689	67046-0689-03
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 100 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1694	67046-1694-03
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 150 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1671	67046-1671-03
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 100 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0764	67046-0764-03
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 25 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1669	67046-1669-03
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 25 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-818	59651-0818-0159651-0818-99
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 150 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-822	59651-0822-01
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 50 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-819	59651-0819-0159651-0819-99
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 75 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-820	59651-0820-01
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 100 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-821	59651-0821-0159651-0821-60

All 201 Amitriptyline Hydrochloride NDCs

Other NDCs under ANDA 213999

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

FDA NDC Directory listings under ANDA 213999
Product	Strength	Form · route	Labeler	Product NDC
Amitriptyline HCL	Amitriptyline hydrochloride 150 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-588
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 10 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-084
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 50 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-334
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 25 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-969
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 25 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1669
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 10 mg/1	Tablet, Film coatedOral	Lifestar Pharma LLC	70756-201
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 25 mg/1	Tablet, Film coatedOral	Lifestar Pharma LLC	70756-202
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 75 mg/1	Tablet, Film coatedOral	Lifestar Pharma LLC	70756-204
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 100 mg/1	Tablet, Film coatedOral	Lifestar Pharma LLC	70756-205
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 150 mg/1	Tablet, Film coatedOral	Lifestar Pharma LLC	70756-206
Amitriptyline Hydrochloride	Amitriptyline hydrochloride 150 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-9710