NDC codes

FDA NDC Directory
Product NDC (as listed)0574-0601Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00574-0601Add 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
0574-0601-1500574060115005740601151 BOTTLE, WITH APPLICATOR in 1 CARTON (0574-0601-15) / 15 mL in 1 BOTTLE, WITH APPLICATORMarketed from Sep 1, 1990

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Podocon 25
Generic name (nonproprietary)
podophyllum resin
Active ingredients
Podophyllum resin — 1 mg/4mL
Dosage form
Tincture
Route
Topical
Labeler
Padagis US LLCNDC labeler code 0574
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 0574-0601_e2ac9612-bded-4eea-a664-f941416583faSPL ID e2ac9612-bded-4eea-a664-f941416583faSPL set ID de96dc6e-e6d1-4383-9ce1-4d06bac08e00UNII 16902YVY2B

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

N400574060115 followed by a unit qualifier and the quantity

Package 00574-0601-15. 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: Podocon-25 ® (25% podophyllin in benzoin tincture) is indicated for the removal of soft genital (venereal) warts (condylomata acuminata) (4) .

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0574-0601

What is NDC 0574-0601?
0574-0601 is the product NDC for Podocon 25 (podophyllum resin), Podophyllum resin 1 mg/4mL tincture, listed with the FDA by Padagis US LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Podocon 25 (Podophyllum resin).
What is the active ingredient?
Podophyllum resin.
Who is the labeler?
Padagis US LLC, NDC labeler code 0574. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Podocon 25?
3 other product NDCs are listed under this name. See all Podocon 25 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 Podocon 25 NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Podocon 25podophyllum resinPodophyllum resin 1 mg/4mLTinctureTopicalBryant Ranch Prepack63629-869963629-8699-01
Podocon 25podophyllum resinPodophyllum resin 1 mg/4mLTinctureTopicalBryant Ranch Prepack71335-292571335-2925-01
Podocon 25podophyllum resinPodophyllum resin 1 mg/4mLTinctureTopicalBryant Ranch Prepack72162-111772162-1117-02

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