What is NDC 69238-1662?

69238-1662 is the product NDC for Scopolamine, Scopolamine 1 mg/3d patch, extended release, listed with the FDA by Amneal Pharmaceuticals NY LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.

Amneal Pharmaceuticals NY LLC, NDC labeler code 69238. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Scopolamine?

13 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Scopolamine NDC 69238-1662 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)69238-1662Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69238-1662Add 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
69238-1662-2	6923816620269238166202	10 PATCH in 1 CARTON (69238-1662-2) / 3 d in 1 PATCHMarketed from Jun 11, 2025
69238-1662-4	6923816620469238166204	24 PATCH in 1 CARTON (69238-1662-4) / 3 d in 1 PATCHMarketed from Jun 11, 2025
69238-1662-9	6923816620969238166209	4 PATCH in 1 CARTON (69238-1662-9) / 3 d in 1 PATCHMarketed from Jun 11, 2025

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): Scopolamine
Generic name (nonproprietary): scopolamine
Active ingredients: Scopolamine — 1 mg/3d
Dosage form: Patch, Extended release
Route: Transdermal
Labeler: Amneal Pharmaceuticals NY LLCNDC labeler code 69238
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218384
Marketing start: Jun 11, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Cholinergic Antagonists (Mechanism)
Identifiers: Product ID 69238-1662_eef82f5e-a712-475a-9206-91891d462beeSPL ID eef82f5e-a712-475a-9206-91891d462beeSPL set ID 48e6e53a-d904-475b-84dd-6068cc0cb36bRxCUI 226552UNII DL48G20X8XUPC 0369238166217
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

N469238166202 followed by a unit qualifier and the quantity

Package 69238-1662-02. 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 May 1, 2025.

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)

About NDC 69238-1662

What is NDC 69238-1662?: 69238-1662 is the product NDC for Scopolamine, Scopolamine 1 mg/3d patch, extended release, listed with the FDA by Amneal Pharmaceuticals NY LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Scopolamine.
What is the active ingredient?: Scopolamine.
Who is the labeler?: Amneal Pharmaceuticals NY LLC, NDC labeler code 69238. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Scopolamine?: 13 other product NDCs are listed under this name. See all Scopolamine 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 Scopolamine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Scopolamine	Scopolamine 1 mg/3d	Patch, Extended releaseTransdermal	Rhodes Pharmaceuticals LLC	42858-150	42858-0150-1442858-0150-4042858-0150-70
Scopolamine	Scopolamine 1 mg/3d	Patch, Extended releaseTransdermal	Bryant Ranch Prepack	71335-3013	71335-3013-01
Scopolamine	Scopolamine 1 mg/3d	Patch, Extended releaseTransdermal	Bryant Ranch Prepack	71335-3014	71335-3014-01
Scopolamine	Scopolamine 1 mg/3d	Patch, Extended releaseTransdermal	Bryant Ranch Prepack	71335-3015	71335-3015-01
Scopolamine	Scopolamine 1 mg/3d	Patch, Extended releaseTransdermal	Bryant Ranch Prepack	72162-2453	72162-2453-0272162-2453-0472162-2453-07
Scopolamine	Scopolamine 1 mg/3d	Patch, Extended releaseTransdermal	Zydus Pharmaceuticals USA Inc.	70710-1846	70710-1846-0270710-1846-0470710-1846-07
Scopolamine	Scopolamine 1 mg/3d	Patch, Extended releaseTransdermal	Zydus Lifesciences Limited	70771-1787	70771-1787-0270771-1787-0470771-1787-07
scopolamine	Scopolamine 1 mg/3d	SystemTransdermal	Actavis Pharma, Inc.	0591-2258	00591-2258-0400591-2258-2300591-2258-79
scopolamine	Scopolamine 1 mg/3d	SystemTransdermal	A-S Medication Solutions	50090-7188	50090-7188-00
Scopolamine	Scopolamine 1.5 mg/1	Patch, Extended releaseTransdermal	Ingenus Pharmaceuticals, LLC	50742-505	50742-0505-0450742-0505-1050742-0505-24

All 14 Scopolamine NDCs