What is NDC 73352-051?

73352-051 is the product NDC for Pruradik (crotamiton), Crotamiton 100 mg/g lotion, listed with the FDA by Trifluent Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Trifluent Pharma, LLC, NDC labeler code 73352. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pruradik?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Pruradik NDC 73352-051 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)73352-051Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73352-0051Add 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	Copy
73352-051-10	7335200511073352005110	237 g in 1 BOTTLE, PLASTIC (73352-051-10)Marketed from Jun 2, 2025

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): Pruradik
Generic name (nonproprietary): crotamiton
Active ingredients: Crotamiton — 100 mg/g
Dosage form: Lotion
Route: Topical
Labeler: Trifluent Pharma, LLCNDC labeler code 73352
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 087204
Marketing start: Jun 2, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 73352-051_36991086-14b5-9e66-e063-6394a90ad654SPL ID 36991086-14b5-9e66-e063-6394a90ad654SPL set ID 3699175f-bfc8-a047-e063-6394a90a80d1RxCUI 106219UNII D6S4O4XD0HUPC 0373352051106

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

NDC on a medical claim

N473352005110 followed by a unit qualifier and the quantity

Package 73352-0051-10. 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 Jun 2, 2025.

Indications (excerpt from the label)

Pruradik ™ (crotamiton USP 10%) is a scabicidal and antipruritic agent as a lotion for topical use only. Crotamiton is a colorless to slightly yellowish oil, having a faint amine-like odor. It is miscible with alcohol and with methanol. Crotamiton is a mixture of the cis and trans isomers. Its molecular weight is 203. 28. Crotamiton is N-ethyl-N(o-methyl-phenyl) 2-butenamide and its structural formula is: Pruradik lotion contains crotamiton USP 10% (100mg/ml) in a creamy lotion base containing purified water, light mineral oil, propylene glycol, cetearyl alcohol (and) cetearth-20, cetyl alcohol, lanolin, benzyl alcohol, carbomer 971P, sodium hydroxide with citric acid (for pH adjustment). im…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73352-051

What is NDC 73352-051?: 73352-051 is the product NDC for Pruradik (crotamiton), Crotamiton 100 mg/g lotion, listed with the FDA by Trifluent Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pruradik (Crotamiton).
What is the active ingredient?: Crotamiton.
Who is the labeler?: Trifluent Pharma, LLC, NDC labeler code 73352. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pruradik?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under ANDA 087204

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

FDA NDC Directory listings under ANDA 087204
Product	Strength	Form · route	Labeler	Product NDC
Crotancrotamiton	Crotamiton 100 mg/g	LotionTopical	Marnel Pharmaceuticals, Inc.	0682-0051

Pruradik (Crotamiton) NDC 73352-051