NDC codes

FDA NDC Directory
Product NDC (as listed)45802-580Labeler and product segments. Claims need a package NDC.
Product NDC at billing width45802-0580Add 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
45802-580-464580205804610 POUCH in 1 CARTON (45802-580-46) / 1 PATCH, EXTENDED RELEASE in 1 POUCHMarketed from Jun 13, 2017
45802-580-624580205806224 POUCH in 1 CARTON (45802-580-62) / 1 PATCH, EXTENDED RELEASE in 1 POUCHMarketed from Jun 13, 2017
45802-580-84458020580844 POUCH in 1 CARTON (45802-580-84) / 1 PATCH, EXTENDED RELEASE in 1 POUCHMarketed from Jun 13, 2017

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)
Scopolamine Transdermal System
Generic name (nonproprietary)
scopolamine transdermal system
Active ingredients
Scopolamine — 1 mg/1
Dosage form
Patch, Extended release
Route
Transdermal
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078830
Marketing start
Marketing end
Other FDA classes
Cholinergic Antagonists (Mechanism)
Identifiers
Product ID 45802-580_d334a21d-7546-477f-a66a-f95b2cf523ceSPL ID d334a21d-7546-477f-a66a-f95b2cf523ceSPL set ID cb93bfad-3e37-4a27-92f6-f21703ae7bdfRxCUI 226552UNII DL48G20X8X
Pharmacologic class
Anticholinergic

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. Transdermal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N445802058046 followed by a unit qualifier and the quantity

Package 45802-0580-46. 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)

Scopolamine transdermal system is indicated in adults for the prevention of: • nausea and vomiting associated with motion sickness. • post-operative nausea and vomiting (PONV) associated with recovery from anesthesia and/or opiate analgesia and surgery. Scopolamine transdermal system is an anticholinergic indicated in adults for the prevention of: • nausea and vomiting associated with motion sickness. ( 1 ) • post-operative nausea and vomiting (PONV) associated with recovery from anesthesia and/or opiate analgesia and surgery. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 078830

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

FDA NDC Directory listings under ANDA 078830
ProductStrengthForm · routeLabelerProduct NDC
Scopolamine Trandermal Systemscolopamine transdermal systemScopolamine 1 mg/1Patch, Extended releaseTransdermalBryant Ranch Prepack63629-8450
Scopolamine Trandermal Systemscolopamine transdermal systemScopolamine 1 mg/1Patch, Extended releaseTransdermalBryant Ranch Prepack63629-8451
Scopolamine Trandermal Systemscolopamine transdermal systemScopolamine 1 mg/1Patch, Extended releaseTransdermalBryant Ranch Prepack63629-8452
Scopolamine Trandermal Systemscolopamine transdermal systemScopolamine 1 mg/1Patch, Extended releaseTransdermalBryant Ranch Prepack72162-1419
Scopolamine Transdermal SystemScopolamine 1 mg/1Patch, Extended releaseTransdermalBryant Ranch Prepack71335-2718

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