What is NDC 42806-029?

42806-029 is the product NDC for Amphetamine Sulfate, Amphetamine sulfate 5 mg/1 tablet, listed with the FDA by Epic Pharma LLC. It has 1 package NDC, 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 Amphetamine Sulfate?

32 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Amphetamine Sulfate NDC 42806-029 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)42806-029Labeler and product segments. Claims need a package NDC.

Product NDC at billing width42806-0029Add 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
42806-029-01	42806002901	100 TABLET in 1 BOTTLE (42806-029-01)Marketed from Sep 18, 2020

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): Amphetamine Sulfate
Generic name (nonproprietary): amphetamine sulfate
Active ingredients: Amphetamine sulfate — 5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Epic Pharma LLCNDC labeler code 42806
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213980
Marketing start: Sep 18, 2020
Listing expires: Dec 31, 2026
DEA schedule: CII
Other FDA classes: Central Nervous System Stimulation (Physiologic effect)
Identifiers: Product ID 42806-029_82a8caba-ccaa-4ff8-8590-9e0b97f7d5f2SPL ID 82a8caba-ccaa-4ff8-8590-9e0b97f7d5f2SPL set ID 432db708-91b7-4802-88c3-ceef597b91daRxCUI 884655, 1600695UNII 6DPV8NK46SUPC 0342806030011, 0342806029015
Pharmacologic class: Central Nervous System Stimulant

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

N442806002901 followed by a unit qualifier and the quantity

Package 42806-0029-01. 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 17, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Amphetamine sulfate tablets, USP are indicated for: 1. Narcolepsy 2. Attention Deficit Disorder with Hyperactivity as an integral part of a total treatment program which typically includes other remedial measures (psychological, educational, social) for a stabilizing effect in children with behavioral syndrome characterized by the following group of developmentally inappropriate symptoms: moderate to severe distractibility, short attention span, hyperactivity, emotional lability, and impulsivity. The diagnosis of the syndrome should not be made with finality when these symptoms are only of comparatively recent origin. Nonlocalizing (soft) neurological signs, learning di…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 42806-029

What is NDC 42806-029?: 42806-029 is the product NDC for Amphetamine Sulfate, Amphetamine sulfate 5 mg/1 tablet, listed with the FDA by Epic Pharma LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Amphetamine Sulfate.
What is the active ingredient?: Amphetamine sulfate.
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 Amphetamine Sulfate?: 32 other product NDCs are listed under this name. See all Amphetamine Sulfate 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 Amphetamine Sulfate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Amphetamine Sulfate	Amphetamine sulfate 5 mg/1	TabletOral	Amici Pharma, Inc.	69292-106	69292-0106-01
Amphetamine Sulfateamphetamine sulfate tablets	Amphetamine sulfate 10 mg/1	TabletOral	Amici Pharma, Inc.	69292-107	69292-0107-01
Amphetamine Sulfate	Amphetamine sulfate 5 mg/1	TabletOral	SpecGx LLC	0406-1219	00406-1219-01
Amphetamine Sulfate	Amphetamine sulfate 10 mg/1	TabletOral	SpecGx LLC	0406-1220	00406-1220-01
Amphetamine Sulfate	Amphetamine sulfate 10 mg/1	TabletOral	Epic Pharma LLC	42806-030	42806-0030-01
Amphetamine Sulfate	Amphetamine sulfate 10 mg/1	TabletOral	Bryant Ranch Prepack	63629-1114	63629-1114-01
Amphetamine Sulfate	Amphetamine sulfate 5 mg/1	TabletOral	Bryant Ranch Prepack	63629-1115	63629-1115-01
Amphetamine Sulfate	Amphetamine sulfate 5 mg/1	TabletOral	Lannett Company, Inc.	0527-2524	00527-2524-37
Amphetamine Sulfate	Amphetamine sulfate 10 mg/1	TabletOral	Lannett Company, Inc.	0527-2525	00527-2525-37
Amphetamine Sulfate	Amphetamine sulfate 10 mg/1	TabletOral	Bryant Ranch Prepack	63629-2078	63629-2078-01

All 33 Amphetamine Sulfate NDCs

Other NDCs under ANDA 213980

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

FDA NDC Directory listings under ANDA 213980
Product	Strength	Form · route	Labeler	Product NDC
Amphetamine Sulfate	Amphetamine sulfate 10 mg/1	TabletOral	Epic Pharma LLC	42806-030