What is NDC 48951-8002?

48951-8002 is the product NDC for Pancreas Equisetum, Sus scrofa pancreas 5 [hp_X]/mL + 2 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?

Sus scrofa pancreas, Quercus robur whole, Equisetum arvense top.

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 Pancreas Equisetum?

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.

Pancreas Equisetum NDC 48951-8002 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-8002Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-8002Add 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
48951-8002-1	4895180020148951800201	10 AMPULE in 1 BOX (48951-8002-1) / 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): Pancreas Equisetum
Generic name (nonproprietary): pancreas equisetum
Active ingredients: Sus scrofa pancreas — 5 [hp_X]/mLQuercus robur whole — 5 [hp_X]/mLEquisetum arvense top — 6 [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, 2027
Identifiers: Product ID 48951-8002_49ef4761-1a55-e16b-e063-6394a90a6297SPL ID 49ef4761-1a55-e16b-e063-6394a90a6297SPL set ID 7920248d-bb69-4403-8b79-1a60c4c70db6UNII 9Y3J3362RY, R7QMG0BT2W, 1DP6Y6B65Z

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

N448951800201 followed by a unit qualifier and the quantity

Package 48951-8002-01. 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 Feb 3, 2026.

Indications (excerpt from the label)

FOR ORAL USE ONLY

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 48951-8002

What is NDC 48951-8002?: 48951-8002 is the product NDC for Pancreas Equisetum, Sus scrofa pancreas 5 [hp_X]/mL + 2 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?: Pancreas Equisetum.
What is the active ingredient?: Sus scrofa pancreas, Quercus robur whole, Equisetum arvense top.
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 Pancreas Equisetum?: 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.