What is NDC 48951-2150?

48951-2150 is the product NDC for Bryophyllum Conchae, Kalanchoe daigremontiana leaf 5 [hp_X]/mL; Ostrea edulis shell 7 [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 is the active ingredient?

Kalanchoe daigremontiana leaf, Ostrea edulis shell.

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 Conchae?

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.

Bryophyllum Conchae NDC 48951-2150

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-2150Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-2150Add 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
48951-2150-1	4895121500148951215001	10 AMPULE in 1 BOX (48951-2150-1) / 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): Bryophyllum Conchae
Generic name (nonproprietary): bryophyllum conchae
Active ingredients: Kalanchoe daigremontiana leaf — 5 [hp_X]/mLOstrea edulis shell — 7 [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 48951-2150_49ef0c70-bb9d-a64a-e063-6394a90a7818SPL ID 49ef0c70-bb9d-a64a-e063-6394a90a7818SPL set ID 12dc3914-21de-7ea3-e063-6294a90aa15fUNII L6X13JKL8O, 49OY13BE7Z

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

N448951215001 followed by a unit qualifier and the quantity

Package 48951-2150-01. 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 48951-2150

What is NDC 48951-2150?: 48951-2150 is the product NDC for Bryophyllum Conchae, Kalanchoe daigremontiana leaf 5 [hp_X]/mL; Ostrea edulis shell 7 [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?: Bryophyllum Conchae.
What is the active ingredient?: Kalanchoe daigremontiana leaf, Ostrea edulis shell.
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 Conchae?: 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.