Age Defiance Pro NDC 44911-0474

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0474Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0474Add 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
44911-0474-1	44911047401	30 mL in 1 BOTTLE, DROPPER (44911-0474-1)Marketed from Sep 24, 2018

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): Age Defiance Pro
Generic name (nonproprietary): 7-oxo-dehydroepiandrosterone-3b-acetate, calcarea carbonica, conium maculatum, glandula suprarenalis suis, hepar suis, hydrofluoricum acidum, hypophysis suis, lycopodium clavatum, selenium metallicum, sepia, silicea, human growth hormone
Active ingredients: 7-oxodehydroepiandrosterone 3-acetate — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLSus scrofa adrenal gland — 12 [hp_X]/mLPork liver — 12 [hp_X]/mLHydrofluoric acid — 12 [hp_X]/mLSus scrofa pituitary gland — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLSomatropin — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 24, 2018
Marketing end: Dec 11, 2028
Other FDA classes: Human Growth Hormone (Chemical structure)
Identifiers: Product ID 44911-0474_e933429b-97d6-49dd-bf20-f5f6a3cf2e5bSPL ID e933429b-97d6-49dd-bf20-f5f6a3cf2e5bSPL set ID d528bdbe-fb75-4b13-9cbc-efa2177d74d8UNII 84RQ0XOM11, 2E32821G6I, Q28R5GF371, 398IYQ16YV, 6EC706HI7F, RGL5YE86CZ, L0PFEMQ1DT, C88X29Y479, H6241UJ22B, QDL83WN8C2, ETJ7Z6XBU4, NQX9KB6PCLUPC 0363113700008
Pharmacologic class: Recombinant Human Growth Hormone

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

N444911047401 followed by a unit qualifier and the quantity

Package 44911-0474-01. 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 May 6, 2026.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms associated with premature aging, such as fatigue, loss of strength, aging skin, varicose veins, sleeplessness 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)