NDC codes

FDA NDC Directory
Product NDC (as listed)83107-018Labeler and product segments. Claims need a package NDC.
Product NDC at billing width83107-0018Add 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
83107-018-018310700180128.4 g in 1 TUBE, WITH APPLICATOR (83107-018-01)Marketed from Jun 23, 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)
Analpram HC
Generic name (nonproprietary)
hydrocortisone acetate and pramoxine hydrochloride
Active ingredients
Hydrocortisone acetate — 10 mg/gPramoxine hydrochloride — 10 mg/g
Dosage form
Cream
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 085368
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 83107-018_38578221-05d3-cc41-e063-6394a90ac88dSPL ID 38578221-05d3-cc41-e063-6394a90ac88dSPL set ID 39618fc5-87a8-47bc-93fc-cb97b8f663c8RxCUI 1235049, 1360954UNII 3X7931PO74, 88AYB867L5UPC 0383107018018
Pharmacologic class
Corticosteroid

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

N483107001801 followed by a unit qualifier and the quantity

Package 83107-0018-01. 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: Topical corticosteroids are indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 085368

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

FDA NDC Directory listings under ANDA 085368
ProductStrengthForm · routeLabelerProduct NDC
hydrocortisone acetate pramoxine hclHydrocortisone acetate 1 g/100g; Pramoxine hydrochloride 1 g/100gCreamTopicalBryant Ranch Prepack72162-1399
hydrocortisone acetate pramoxine hclHydrocortisone acetate 1 g/100g; Pramoxine hydrochloride 1 g/100gCreamTopicalPadagis Israel Pharmaceuticals Ltd45802-144
hydrocortisone acetate pramoxine hclHydrocortisone acetate 1 g/100g; Pramoxine hydrochloride 1 g/100gCreamTopicalBryant Ranch Prepack63629-8669
Pramosone Creamhydrocortisone acetate and pramoxine hydrochlorideHydrocortisone acetate 10 mg/g; Pramoxine hydrochloride 10 mg/gCreamTopicalLegacy Pharma USA Inc.83107-017
Pramosone Creamhydrocortisone acetate and pramoxine hydrochlorideHydrocortisone acetate 10 mg/g; Pramoxine hydrochloride 10 mg/gCreamTopicalLegacy Pharma USA Inc.83107-016

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