Lymphastat NDC 44911-0615

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0615Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0615Add 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
44911-0615-1	44911061501	30 mL in 1 BOTTLE, DROPPER (44911-0615-1)Marketed from May 25, 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): Lymphastat
Generic name (nonproprietary): baptisia tinctoria, echinacea (angustifolia), lobelia inflata, lomatium dissectum, hydrastis canadensis, lung (suis), phytolacca decandra, symphytum officinale, aconitum napellus, arsenicum album, belladonna, bryonia (alba), causticum, eupatorium perfoliatum, ferrum phosphoricum, gelsemium sempervirens, hypericum perforatum, kali carbonicum, lachesis mutus, natrum sulphuricum, phosphorus, pulsatilla (pratensis), rhus tox, silicea, sulphur, pyrogenium
Active ingredients: Baptisia tinctoria root — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLLobelia inflata whole — 3 [hp_X]/mLLomatium dissectum root — 3 [hp_X]/mLGoldenseal — 6 [hp_X]/mLSus scrofa lung — 6 [hp_X]/mLPhytolacca americana root — 6 [hp_X]/mLComfrey root — 6 [hp_X]/mLAconitum napellus whole — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLCausticum — 12 [hp_X]/mLEupatorium perfoliatum flowering top — 12 [hp_X]/mLFerrosoferric phosphate — 12 [hp_X]/mLGelsemium sempervirens root — 12 [hp_X]/mLHypericum perforatum whole — 12 [hp_X]/mLPotassium carbonate — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLSodium sulfate — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLRancid beef — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Prescription drug
Marketing category: Unapproved homeopathic
Marketing start: May 25, 2021
Marketing end: May 8, 2028
Identifiers: Product ID 44911-0615_56d34b51-8210-4595-8124-db99399cb794SPL ID 56d34b51-8210-4595-8124-db99399cb794SPL set ID ed3e0362-a4d3-46fa-a045-17bf659b777cUNII 5EF0HWI5WU, VB06AV5US8, 9PP1T3TC5U, 5329928G5N, ZW3Z11D0JV, 7GL3G1COB3, 11E6VI8VEG, M9VVZ08EKQ, U0NQ8555JD, S7V92P67HO, WQZ3G9PF0H, T7J046YI2B, DD5FO1WKFU, 1W0775VX6E, 91GQH8I5F7, 639KR60Q1Q, XK4IUX8MNB, BQN1B9B9HA, VSW71SS07I, 0YPR65R21J, 27YLU75U4W, 8E272251DI, 6IO182RP7A, ETJ7Z6XBU4, 70FD1KFU70, 29SUH5R3HUUPC 0363113700640

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

N444911061501 followed by a unit qualifier and the quantity

Package 44911-0615-01. 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 Oct 28, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms associated with viral and bacterial infections, such as fever, irritated throat, and cough with tickle in the throat.** **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)