What is NDC 48951-8425?

48951-8425 is the product NDC for Pulmo Mercurius, Sus scrofa lung 8 [hp_X]/mL; Mercury 17 [hp_X]/mL liquid, listed with the FDA by Uriel Pharmacy Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Uriel Pharmacy Inc., NDC labeler code 48951. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pulmo Mercurius?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Pulmo Mercurius NDC 48951-8425 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-8425Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-8425Add 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
48951-8425-3	4895184250348951842503	60 mL in 1 BOTTLE, DROPPER (48951-8425-3)Marketed from Sep 1, 2009

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): Pulmo Mercurius
Generic name (nonproprietary): pulmo mercurius
Active ingredients: Sus scrofa lung — 8 [hp_X]/mLMercury — 17 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Uriel Pharmacy Inc.NDC labeler code 48951
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 1, 2009
Listing expires: Dec 31, 2026
Identifiers: Product ID 48951-8425_43e5678b-2e4f-6b11-e063-6394a90ab886SPL ID 43e5678b-2e4f-6b11-e063-6394a90ab886SPL set ID 2889ec85-faab-21ab-e063-6394a90aaedaUNII 7GL3G1COB3, FXS1BY2PGL

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

NDC on a medical claim

N448951842503 followed by a unit qualifier and the quantity

Package 48951-8425-03. 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 Nov 18, 2025.

Indications (excerpt from the label)

Directions: FOR ORAL USE ONLY.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 48951-8425

What is NDC 48951-8425?: 48951-8425 is the product NDC for Pulmo Mercurius, Sus scrofa lung 8 [hp_X]/mL; Mercury 17 [hp_X]/mL liquid, listed with the FDA by Uriel Pharmacy Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pulmo Mercurius.
What is the active ingredient?: Sus scrofa lung, Mercury.
Who is the labeler?: Uriel Pharmacy Inc., NDC labeler code 48951. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pulmo Mercurius?: 1 other product NDC are listed under this name. See all Pulmo Mercurius 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 Pulmo Mercurius NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Pulmo Mercurius	Sus scrofa lung 8 [hp_X]/mL; Mercury 17 [hp_X]/mL	LiquidOral	Uriel Pharmacy Inc.	48951-8089	48951-8089-01