Anger NDC 50845-0269

NDC codes

FDA NDC Directory

Product NDC (as listed)50845-0269Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50845-0269Add 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
50845-0269-2	50845026902	1 BOTTLE, SPRAY in 1 CARTON (50845-0269-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0269-1)Marketed from Feb 23, 2021

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): Anger
Generic name (nonproprietary): aconitum napellus, asafoetida, chamomilla, crocus sativus, hyoscyamus niger, ignatia amara, staphysagria, valeriana officinalis
Active ingredients: Aconitum napellus whole — 200 [hp_C]/mLFerula assa-foetida resin — 4 [hp_X]/mLMatricaria chamomilla whole — 3 [hp_X]/mLSaffron — 3 [hp_X]/mLHyoscyamus niger — 200 [hp_C]/mLStrychnos ignatii seed — 4 [hp_X]/mLDelphinium staphisagria seed — 200 [hp_C]/mLValerian — 3 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: Liddell Laboratories
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 23, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 50845-0269_cdb4274e-5d6d-441c-a283-e8252e696d3dSPL ID cdb4274e-5d6d-441c-a283-e8252e696d3dSPL set ID a427f6fe-606f-4248-8f9d-60aa4ba4765bUNII U0NQ8555JD, W9FZA51AS1, G0R4UBI2ZZ, E849G4X5YJ, 4WRK2153H3, 1NM3M2487K, 00543AP1JV, JWF5YAW3QWUPC 0363113272963

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

N450845026902 followed by a unit qualifier and the quantity

Package 50845-0269-02. 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 Dec 1, 2023.

Indications (excerpt from the label)

USES: May temporarily relieve symptoms of anger, such as: explosive outbursts feelings of hostility restlessness irritability** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)