NDC codes

FDA NDC Directory
Product NDC (as listed)72162-1087Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-1087Add 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 NDC11-digit (billing)PackageCopy
72162-1087-172162108701100 TABLET in 1 BOTTLE (72162-1087-1)Marketed from Apr 5, 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)
Amphetamine Sulfate
Generic name (nonproprietary)
amphetamine sulfate
Active ingredients
Amphetamine sulfate5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212901
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Central Nervous System Stimulation (Physiologic effect)
Identifiers
Product ID 72162-1087_698171ee-4328-476a-b71c-58aa6dc93b23SPL ID 698171ee-4328-476a-b71c-58aa6dc93b23SPL set ID 698171ee-4328-476a-b71c-58aa6dc93b23RxCUI 884655UNII 6DPV8NK46S

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

N472162108701 followed by a unit qualifier and the quantity

Package 72162-1087-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Amphetamine sulfate tablets, USP 5 mg and 10 mg are indicated for: Narcolepsy 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, le

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 212901

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

FDA NDC Directory listings under ANDA 212901
ProductStrengthForm · routeLabelerProduct NDC
Amphetamine SulfateAmphetamine sulfate 5 mg/1TabletOralLannett Company, Inc.0527-2524
Amphetamine SulfateAmphetamine sulfate 10 mg/1TabletOralBryant Ranch Prepack72162-1088
Amphetamine SulfateAmphetamine sulfate 10 mg/1TabletOralLannett Company, Inc.0527-2525
Amphetamine SulfateAmphetamine sulfate 10 mg/1TabletOralBryant Ranch Prepack71335-2990
Amphetamine SulfateAmphetamine sulfate 5 mg/1TabletOralAmici Pharma, Inc.69292-106
Amphetamine Sulfateamphetamine sulfate tabletsAmphetamine sulfate 10 mg/1TabletOralAmici Pharma, Inc.69292-107
Amphetamine SulfateAmphetamine sulfate 5 mg/1TabletOralBryant Ranch Prepack63629-2079
Amphetamine SulfateAmphetamine sulfate 10 mg/1TabletOralBryant Ranch Prepack63629-2078

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in