What is NDC 48951-6012?

48951-6012 is the product NDC for Lachesis Belladonna, Atropa belladonna 4 [hp_X]/mL + 3 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?

Atropa belladonna, Mercurialis perennis, Calcium sulfide, Lachesis muta venom.

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 Lachesis Belladonna?

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.

Lachesis Belladonna NDC 48951-6012

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-6012Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-6012Add 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
48951-6012-1	4895160120148951601201	10 AMPULE in 1 BOX (48951-6012-1) / 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): Lachesis Belladonna
Generic name (nonproprietary): lachesis belladonna
Active ingredients: Atropa belladonna — 4 [hp_X]/mLMercurialis perennis — 6 [hp_X]/mLCalcium sulfide — 7 [hp_X]/mLLachesis muta venom — 12 [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 48951-6012_2b24df98-1d29-5f7b-e063-6294a90a423aSPL ID 2b24df98-1d29-5f7b-e063-6294a90a423aSPL set ID c617a849-5043-43cd-974f-2f0d664fd468UNII WQZ3G9PF0H, Q35465A1MA, 1MBW07J51Q, VSW71SS07I

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

N448951601201 followed by a unit qualifier and the quantity

Package 48951-6012-01. 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 Jan 7, 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 48951-6012

What is NDC 48951-6012?: 48951-6012 is the product NDC for Lachesis Belladonna, Atropa belladonna 4 [hp_X]/mL + 3 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?: Lachesis Belladonna.
What is the active ingredient?: Atropa belladonna, Mercurialis perennis, Calcium sulfide, Lachesis muta venom.
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 Lachesis Belladonna?: 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.