What is NDC 48951-2057?

48951-2057 is the product NDC for Berberis Urtica, Berberis vulgaris root bark 1 [hp_X]/1; Urtica urens 2 [hp_X]/1 pellet, 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?

Berberis vulgaris root bark, Urtica urens.

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 Berberis Urtica?

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.

Berberis Urtica NDC 48951-2057 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-2057Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-2057Add 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
48951-2057-2	4895120570248951205702	1350 PELLET in 1 BOTTLE, GLASS (48951-2057-2)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): Berberis Urtica
Generic name (nonproprietary): berberis urtica
Active ingredients: Berberis vulgaris root bark — 1 [hp_X]/1Urtica urens — 2 [hp_X]/1
Dosage form: Pellet
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 48951-2057_43584a04-748f-db17-e063-6394a90abd2dSPL ID 43584a04-748f-db17-e063-6394a90abd2dSPL set ID a063c6ea-020e-4059-9a6e-14428ce26b6fUNII 1TH8Q20J0U, IHN2NQ5OF9

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

N448951205702 followed by a unit qualifier and the quantity

Package 48951-2057-02. 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 11, 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 48951-2057

What is NDC 48951-2057?: 48951-2057 is the product NDC for Berberis Urtica, Berberis vulgaris root bark 1 [hp_X]/1; Urtica urens 2 [hp_X]/1 pellet, 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?: Berberis Urtica.
What is the active ingredient?: Berberis vulgaris root bark, Urtica urens.
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 Berberis Urtica?: 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.