What is NDC 48951-8084?

48951-8084 is the product NDC for Pulmo Bryonia, Bryonia alba root 6 [hp_X]/mL + 4 more ingredients liquid, listed with the FDA by Uriel Pharmacy Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Bryonia alba root, Gelsemium sempervirens root, Antimony potassium tartrate, Ferrosoferric phosphate, Sus scrofa lung.

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 Bryonia?

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.

Pulmo Bryonia NDC 48951-8084 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-8084Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-8084Add 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
48951-8084-1	4895180840148951808401	10 AMPULE in 1 BOX (48951-8084-1) / 1 mL in 1 AMPULEMarketed 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 Bryonia
Generic name (nonproprietary): pulmo bryonia
Active ingredients: Bryonia alba root — 6 [hp_X]/mLGelsemium sempervirens root — 6 [hp_X]/mLAntimony potassium tartrate — 8 [hp_X]/mLFerrosoferric phosphate — 8 [hp_X]/mLSus scrofa lung — 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 48951-8084_3b540ddb-39ea-80e5-e063-6294a90ad1e3SPL ID 3b540ddb-39ea-80e5-e063-6294a90ad1e3SPL set ID a6752cc7-ff8c-4c34-a0a9-0658a915c8ccUNII T7J046YI2B, 639KR60Q1Q, DL6OZ476V3, 91GQH8I5F7, 7GL3G1COB3

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

N448951808401 followed by a unit qualifier and the quantity

Package 48951-8084-01. 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 Aug 1, 2025.

Indications (excerpt from the label)

Directions: FOR ORAL USE.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 48951-8084

What is NDC 48951-8084?: 48951-8084 is the product NDC for Pulmo Bryonia, Bryonia alba root 6 [hp_X]/mL + 4 more ingredients 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 Bryonia.
What is the active ingredient?: Bryonia alba root, Gelsemium sempervirens root, Antimony potassium tartrate, Ferrosoferric phosphate, Sus scrofa lung.
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 Bryonia?: 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.