Adrenapath NDC 64578-0096

NDC codes

FDA NDC Directory

Product NDC (as listed)64578-0096Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64578-0096Add 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
64578-0096-1	64578009601	59.1 mL in 1 BOTTLE, DROPPER (64578-0096-1)Marketed from Mar 13, 2017

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): Adrenapath
Generic name (nonproprietary): carduus marianus, chelidonium majus, echinacea (angustifolia), glandula suprarenalis suis, natrum muriaticum, phosphoricum acidum, pituitarum posterium (bovine), thyroidinum (bovine)
Active ingredients: Milk thistle — 12 [hp_X]/mLChelidonium majus — 4 [hp_X]/mLEchinacea angustifolia — 4 [hp_X]/mLSus scrofa adrenal gland — 9 [hp_X]/mLSodium chloride — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLBos taurus pituitary gland — 12 [hp_X]/mLThyroid, Bovine — 9 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energetix Corporation
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 13, 2017
Listing expires: Dec 31, 2027
Identifiers: Product ID 64578-0096_58c87689-8864-6e2f-e063-6294a90a9ac3SPL ID 58c87689-8864-6e2f-e063-6294a90a9ac3SPL set ID c300b8f5-4334-4597-a303-8200cbc117d1UNII U946SH95EE, 7E889U5RNN, VB06AV5US8, 398IYQ16YV, 451W47IQ8X, E4GA8884NN, 7JM57I419K, MN18OTN73W

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

N464578009601 followed by a unit qualifier and the quantity

Package 64578-0096-01. 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 11, 2026.

Indications (excerpt from the label)

Uses Temporary relief of exhaustion, cravings, restless sleep.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)