NDC codes

FDA NDC Directory
Product NDC (as listed)48951-8140Labeler and product segments. Claims need a package NDC.
Product NDC at billing width48951-8140Add 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 NDC11-digit (billing)PackageCopy
48951-8140-1489518140014895181400110 AMPULE in 1 BOX (48951-8140-1) / 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)
Rhus Aconitum
Generic name (nonproprietary)
rhus aconitum
Active ingredients
Gelsemium sempervirens root — 4 [hp_X]/mLPseudognaphalium luteoalbum leaf — 4 [hp_X]/mLAconitum napellus — 6 [hp_X]/mLAtropa belladonna — 6 [hp_X]/mLMandragora officinarum root — 6 [hp_X]/mLToxicodendron pubescens leaf — 6 [hp_X]/mLPenoxsulam — 10 [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
Listing expires
Identifiers
Product ID 48951-8140_4bd37192-f7e8-b961-e063-6294a90ab3d3SPL ID 4bd37192-f7e8-b961-e063-6294a90ab3d3SPL set ID a176c241-fc2d-4fea-82d9-81183971b4cfUNII 639KR60Q1Q, BGI20Z6M57, U0NQ8555JD, WQZ3G9PF0H, I2XCB174VB, 6IO182RP7A, 784ELC1SCZ

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

N448951814001 followed by a unit qualifier and the quantity

Package 48951-8140-01. 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 .

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 48951-8140

What is NDC 48951-8140?
48951-8140 is the product NDC for Rhus Aconitum, Gelsemium sempervirens root 4 [hp_X]/mL + 6 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?
Rhus Aconitum.
What is the active ingredient?
Gelsemium sempervirens root, Pseudognaphalium luteoalbum leaf, Aconitum napellus, Atropa belladonna, Mandragora officinarum root, Toxicodendron pubescens leaf, Penoxsulam.
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 Rhus Aconitum?
1 other product NDC are listed under this name. See all Rhus Aconitum 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 Rhus Aconitum NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Rhus AconitumGelsemium sempervirens root 3 [hp_X]/1 + 6 more ingredientsPelletOralUriel Pharmacy Inc.48951-814248951-8142-02

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