NDC codes

FDA NDC Directory
Product NDC (as listed)66993-359Labeler and product segments. Claims need a package NDC.
Product NDC at billing width66993-0359Add 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
66993-359-576699303595766993035957473 mL in 1 BOTTLE, PLASTIC (66993-359-57)Marketed from May 15, 2014

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/5mL
Dosage form
Solution
Route
Oral
Labeler
Prasco LaboratoriesNDC labeler code 66993
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040776
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Central Nervous System Stimulation (Physiologic effect)
Identifiers
Product ID 66993-359_48ddaac7-2105-4427-97c8-aca9790ac361SPL ID 48ddaac7-2105-4427-97c8-aca9790ac361SPL set ID 94674695-aa8a-3150-e053-2995a90a445fRxCUI 884522UNII JJ768O327NUPC 0366993359571

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

N466993035957 followed by a unit qualifier and the quantity

Package 66993-0359-57. 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 Dextroamphetamine Sulfate Oral Solution is indicated in: Narcolepsy Attention Deficit Disorder with Hyperactivity: As an integral part of a total treatment program that typically includes other remedial measures (psychological, educational, social) for a stabilizing effect in pediatric patients (ages 3 years to 16 years) with a behavioral syndrome characterized by the following group of developmentally inappropriate symptoms: Moderate to severe distractibility, short attention span, hyperactivity, emotionally lability, and impulsivity. The diagnosis of this syndrome should not be made with finality when these symptoms are only of comparatively recent origin. Nonlocalizi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 66993-359

What is NDC 66993-359?
66993-359 is the product NDC for Dextroamphetamine Sulfate, Dextroamphetamine sulfate 5 mg/5mL solution, listed with the FDA by Prasco Laboratories. It has 1 package NDC, 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?
Prasco Laboratories, NDC labeler code 66993. 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 040776

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

FDA NDC Directory listings under ANDA 040776
ProductStrengthForm · routeLabelerProduct NDC
Procentradextroamphetamine sulfateDextroamphetamine sulfate 5 mg/5mLSolutionOralINDEPENDENCE PHARMACEUTICALS, LLC21724-701

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