NDC codes

FDA NDC Directory
Product NDC (as listed)10702-065Labeler and product segments. Claims need a package NDC.
Product NDC at billing width10702-0065Add 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
10702-065-011070200650110702006501100 TABLET in 1 BOTTLE (10702-065-01)Marketed from Nov 23, 2015
10702-065-03107020065031070200650330 TABLET in 1 BOTTLE (10702-065-03)Marketed from Nov 23, 2015
10702-065-06107020065061070200650660 TABLET in 1 BOTTLE (10702-065-06)Marketed from Nov 23, 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)
Dextroamphetamine Sulfate
Generic name (nonproprietary)
dextroamphetamine sulfate
Active ingredients
Dextroamphetamine sulfate — 5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
KVK-Tech, Inc.NDC labeler code 10702
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203548
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Central Nervous System Stimulation (Physiologic effect)
Identifiers
Product ID 10702-065_0f296f50-a802-d586-e063-6394a90a4888SPL ID 0f296f50-a802-d586-e063-6394a90a4888SPL set ID 863d66fe-9c38-463a-afa1-552647494c5aRxCUI 884385, 884386UNII JJ768O327NUPC 0310702065017

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

N410702006501 followed by a unit qualifier and the quantity

Package 10702-0065-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Dextroamphetamine 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 pediatric patients (ages 3 to 16 years) with a 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 this syndrome should not be made with finality when these symptoms are only of comparatively recent origin. Nonlocaliz…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 10702-065

What is NDC 10702-065?
10702-065 is the product NDC for Dextroamphetamine Sulfate, Dextroamphetamine sulfate 5 mg/1 tablet, listed with the FDA by KVK-Tech, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Dextroamphetamine Sulfate.
What is the active ingredient?
Dextroamphetamine sulfate.
Who is the labeler?
KVK-Tech, Inc., NDC labeler code 10702. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dextroamphetamine Sulfate?
38 other product NDCs are listed under this name. See all Dextroamphetamine 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 Dextroamphetamine Sulfate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Dextroamphetamine SulfateDextroamphetamine sulfate 5 mg/1TabletOralCranbury Pharmaceuticals, LLC27808-08927808-0089-01
Dextroamphetamine SulfateDextroamphetamine sulfate 10 mg/1TabletOralCranbury Pharmaceuticals, LLC27808-09027808-0090-01
Dextroamphetamine SulfateDextroamphetamine sulfate 2.5 mg/1TabletOralWinder Laboratories LLC75826-12075826-0120-1075826-0120-30
Dextroamphetamine SulfateDextroamphetamine sulfate 5 mg/1TabletOralWinder Laboratories LLC75826-12175826-0121-1075826-0121-30
Dextroamphetamine SulfateDextroamphetamine sulfate 7.5 mg/1TabletOralWinder Laboratories LLC75826-12275826-0122-1075826-0122-30
Dextroamphetamine SulfateDextroamphetamine sulfate 10 mg/1TabletOralWinder Laboratories LLC75826-12375826-0123-1075826-0123-30
Dextroamphetamine SulfateDextroamphetamine sulfate 15 mg/1TabletOralWinder Laboratories LLC75826-12475826-0124-1075826-0124-30
Dextroamphetamine SulfateDextroamphetamine sulfate 20 mg/1TabletOralWinder Laboratories LLC75826-12575826-0125-1075826-0125-30
Dextroamphetamine SulfateDextroamphetamine sulfate 30 mg/1TabletOralWinder Laboratories LLC75826-12675826-0126-1075826-0126-30
Dextroamphetamine SulfateDextroamphetamine sulfate 15 mg/1TabletOralWilshire Pharmaceuticals, Inc.52536-51552536-0515-03

All 39 Dextroamphetamine Sulfate NDCs

Other NDCs under ANDA 203548

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

FDA NDC Directory listings under ANDA 203548
ProductStrengthForm · routeLabelerProduct NDC
Dextroamphetamine SulfateDextroamphetamine sulfate 10 mg/1TabletOralKVK-Tech, Inc.10702-066

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