What is NDC 48951-2165?

48951-2165 is the product NDC for Bryophyllum Argentum, Kalanchoe daigremontiana leaf 3 [hp_X]/1; Silver 6 [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?

Kalanchoe daigremontiana leaf, Silver.

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 Bryophyllum Argentum?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Bryophyllum Argentum NDC 48951-2165

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-2165Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-2165Add 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
48951-2165-2	4895121650248951216502	1350 PELLET in 1 BOTTLE, GLASS (48951-2165-2)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): Bryophyllum Argentum
Generic name (nonproprietary): bryophyllum argentum
Active ingredients: Kalanchoe daigremontiana leaf — 3 [hp_X]/1Silver — 6 [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, 2027
Identifiers: Product ID 48951-2165_5ce1ad6a-afad-e05f-e063-6394a90a7a19SPL ID 5ce1ad6a-afad-e05f-e063-6394a90a7a19

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

N448951216502 followed by a unit qualifier and the quantity

Package 48951-2165-02. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 48951-2165

What is NDC 48951-2165?: 48951-2165 is the product NDC for Bryophyllum Argentum, Kalanchoe daigremontiana leaf 3 [hp_X]/1; Silver 6 [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?: Bryophyllum Argentum.
What is the active ingredient?: Kalanchoe daigremontiana leaf, Silver.
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 Bryophyllum Argentum?: 1 other product NDC are listed under this name. See all Bryophyllum Argentum 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 Bryophyllum Argentum NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Bryophyllum Argentum	Kalanchoe daigremontiana leaf 3 [hp_X]/mL; Silver 6 [hp_X]/mL	LiquidOral	Uriel Pharmacy Inc.	48951-2164	48951-2164-01