What is NDC 23155-952?

23155-952 is the product NDC for Benzphetamine Hydrochloride, Benzphetamine hydrochloride 50 mg/1 tablet, film coated, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Benzphetamine Hydrochloride?

5 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Benzphetamine Hydrochloride NDC 23155-952

NDC codes

FDA NDC Directory

Product NDC (as listed)23155-952Labeler and product segments. Claims need a package NDC.

Product NDC at billing width23155-0952Add 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
23155-952-01	2315509520123155095201	100 TABLET, FILM COATED in 1 BOTTLE (23155-952-01)Marketed from Jun 19, 2026
23155-952-03	2315509520323155095203	30 TABLET, FILM COATED in 1 BOTTLE (23155-952-03)Marketed from Jun 19, 2026
23155-952-05	2315509520523155095205	500 TABLET, FILM COATED in 1 BOTTLE (23155-952-05)Marketed from Jun 19, 2026

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): Benzphetamine Hydrochloride
Generic name (nonproprietary): benzphetamine hydrochloride
Active ingredients: Benzphetamine hydrochloride — 50 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.NDC labeler code 23155
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202061
Marketing start: Jun 19, 2026
Listing expires: Dec 31, 2027
DEA schedule: CIII
Other FDA classes: Appetite Suppression (Physiologic effect)Increased Sympathetic Activity (Physiologic effect)
Identifiers: Product ID 23155-952_e359f1ec-c10f-4752-9b9a-c2fd120c4356SPL ID e359f1ec-c10f-4752-9b9a-c2fd120c4356SPL set ID 152a123e-4886-4184-a47d-462ce102b8faRxCUI 904368UNII 43DWT87QT7UPC 0323155952018, 0323155952056, 0323155952032
Pharmacologic class: Sympathomimetic Amine Anorectic

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

N423155095201 followed by a unit qualifier and the quantity

Package 23155-0952-01. 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 18, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Benzphetamine hydrochloride tablets are indicated in the management of exogenous obesity as a short term (a few weeks) adjunct in a regimen of weight reduction based on caloric restriction in patients with an initial body mass index (BMI) of 30 kg/m 2 or higher who have not responded to appropriate weight reducing regimen (diet and/or exercise) alone. Below is a chart of Body Mass Index (BMI) based on various heights and weights. BMI is calculated by taking the patient's weight, in kilograms (kg), divided by the patient's height, in meters (m), squared. Metric conversions are as follows: pounds ÷2.2 = kg; inches × 0.0254 = meters. The limited usefulness of agents of thi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 23155-952

What is NDC 23155-952?: 23155-952 is the product NDC for Benzphetamine Hydrochloride, Benzphetamine hydrochloride 50 mg/1 tablet, film coated, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Benzphetamine Hydrochloride.
What is the active ingredient?: Benzphetamine hydrochloride.
Who is the labeler?: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Benzphetamine Hydrochloride?: 5 other product NDCs are listed under this name. See all Benzphetamine 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 Benzphetamine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Benzphetamine Hydrochloride	Benzphetamine hydrochloride 50 mg/1	Tablet, Film coatedOral	Epic Pharma, LLC	42806-081	42806-0081-0142806-0081-0542806-0081-30
Benzphetamine Hydrochloride	Benzphetamine hydrochloride 50 mg/1	TabletOral	KVK-TECH, INC	10702-040	10702-0040-0110702-0040-0310702-0040-10+1 more
Benzphetamine Hydrochloride	Benzphetamine hydrochloride 50 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-541	43063-0541-1443063-0541-3043063-0541-45+3 more
Benzphetamine Hydrochloride	Benzphetamine hydrochloride 50 mg/1	TabletOral	Bryant Ranch Prepack	71335-0451	71335-0451-0171335-0451-0271335-0451-03+6 more
benzphetamine hydrochloride	Benzphetamine hydrochloride 50 mg/1	TabletOral	Calvin Scott & Co., Inc.	17224-672	17224-0672-3017224-0672-60