What is NDC 42806-081?

42806-081 is the product NDC for Benzphetamine Hydrochloride, Benzphetamine hydrochloride 50 mg/1 tablet, film coated, listed with the FDA by Epic Pharma, LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.

Epic Pharma, LLC, NDC labeler code 42806. 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 42806-081

NDC codes

FDA NDC Directory

Product NDC (as listed)42806-081Labeler and product segments. Claims need a package NDC.

Product NDC at billing width42806-0081Add 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
42806-081-01	42806008101	100 TABLET, FILM COATED in 1 BOTTLE (42806-081-01)Marketed from Dec 16, 2015
42806-081-05	42806008105	500 TABLET, FILM COATED in 1 BOTTLE (42806-081-05)Marketed from Dec 16, 2015
42806-081-30	42806008130	30 TABLET, FILM COATED in 1 BOTTLE (42806-081-30)Marketed from Dec 16, 2015

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: Epic Pharma, LLCNDC labeler code 42806
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090346
Marketing start: Dec 16, 2015
Listing expires: Dec 31, 2026
DEA schedule: CIII
Other FDA classes: Appetite Suppression (Physiologic effect)Increased Sympathetic Activity (Physiologic effect)
Identifiers: Product ID 42806-081_b4e5d191-8cbf-4111-a07b-025b920269c4SPL ID b4e5d191-8cbf-4111-a07b-025b920269c4SPL set ID f6d9b369-4b64-4d3f-844d-5d60dd257c55RxCUI 904368UNII 43DWT87QT7UPC 0342806081013
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

N442806008101 followed by a unit qualifier and the quantity

Package 42806-0081-01. 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 Dec 27, 2023.

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/m2 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 this…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 42806-081

What is NDC 42806-081?: 42806-081 is the product NDC for Benzphetamine Hydrochloride, Benzphetamine hydrochloride 50 mg/1 tablet, film coated, listed with the FDA by Epic Pharma, LLC. 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?: Epic Pharma, LLC, NDC labeler code 42806. 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	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-952	23155-0952-0123155-0952-0323155-0952-05
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