Adrenapar NDC 44911-0037

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0037Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0037Add 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
44911-0037-1	44911003701	60 mL in 1 BOTTLE, DROPPER (44911-0037-1)Marketed from Oct 4, 2012

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): Adrenapar
Generic name (nonproprietary): aralia quinquefolia, avena sativa, glandula suprarenalis suis, arsenicum iodatum, ignatia amara, lycopodium clavatum, nux vomica, phosphoricum acidum, phosphorus, zincum metallicum
Active ingredients: American ginseng — 3 [hp_X]/mLAvena sativa flowering top — 3 [hp_X]/mLSus scrofa adrenal gland — 6 [hp_X]/mLArsenic triiodide — 12 [hp_X]/mLStrychnos ignatii seed — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLZinc — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 4, 2012
Marketing end: Jan 13, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 44911-0037_122799c5-9bc4-49ca-8935-f31d0db3dbeeSPL ID 122799c5-9bc4-49ca-8935-f31d0db3dbeeSPL set ID 06fccf1a-2a70-4f29-8864-4577e6c39d9bUNII 8W75VCV53Q, MA9CQJ3F7F, 398IYQ16YV, 3029988O2T, 1NM3M2487K, C88X29Y479, 269XH13919, E4GA8884NN, 27YLU75U4W, J41CSQ7QDS
Pharmacologic class: Non-Standardized Plant Allergenic Extract

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

N444911003701 followed by a unit qualifier and the quantity

Package 44911-0037-01. 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 Aug 10, 2022.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve nervous exhaustion, fatigue and forgetfulness.** **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)