What is NDC 63479-2516?

63479-2516 is the product NDC for ENERGY Formula, Phosphoric acid 3 [hp_C]/mL + 5 more ingredients solution/ drops, listed with the FDA by Apex Energetics Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

ENERGY Formula (Adenosine triphosphate, Antimony potassium tartrate, Cinchona officinalis bark, Strychnos nux-vomica seed, Phosphoric acid, Sulfur).

What is the active ingredient?

Phosphoric acid, Strychnos nux-vomica seed, Antimony potassium tartrate, Cinchona officinalis bark, Sulfur, Adenosine triphosphate.

Apex Energetics Inc., NDC labeler code 63479. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for ENERGY Formula?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

ENERGY Formula NDC 63479-2516 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-2516Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-2516Add 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
63479-2516-1	6347925160163479251601	30 mL in 1 BOTTLE, GLASS (63479-2516-1)Marketed from Mar 22, 2022

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): ENERGY Formula
Generic name (nonproprietary): adenosine triphosphate, antimony potassium tartrate, cinchona officinalis bark, strychnos nux-vomica seed, phosphoric acid, sulfur
Active ingredients: Phosphoric acid — 3 [hp_C]/mLStrychnos nux-vomica seed — 1 [hp_Q]/mLAntimony potassium tartrate — 1 [hp_Q]/mLCinchona officinalis bark — 7 [hp_C]/mLSulfur — 2 [hp_Q]/mLAdenosine triphosphate — 6 [hp_X]/mL
Dosage form: Solution/ drops
Route: Sublingual
Labeler: Apex Energetics Inc.NDC labeler code 63479
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 22, 2022
Listing expires: Dec 31, 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 63479-2516_0e774462-818d-9c5d-e063-6294a90affacSPL ID 0e774462-818d-9c5d-e063-6294a90affacSPL set ID d8c773f7-504a-bb56-e053-2a95a90aefccUNII E4GA8884NN, 269XH13919, DL6OZ476V3, S003A158SB, 70FD1KFU70, 8L70Q75FXE
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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463479251601 followed by a unit qualifier and the quantity

Package 63479-2516-01. 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 Jan 8, 2024.

Indications (excerpt from the label)

Uses: For temporary relief of minor: fatigue* irritability* muscle weakness* dizziness* indigestion* *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)

About NDC 63479-2516

What is NDC 63479-2516?: 63479-2516 is the product NDC for ENERGY Formula, Phosphoric acid 3 [hp_C]/mL + 5 more ingredients solution/ drops, listed with the FDA by Apex Energetics Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: ENERGY Formula (Adenosine triphosphate, Antimony potassium tartrate, Cinchona officinalis bark, Strychnos nux-vomica seed, Phosphoric acid, Sulfur).
What is the active ingredient?: Phosphoric acid, Strychnos nux-vomica seed, Antimony potassium tartrate, Cinchona officinalis bark, Sulfur, Adenosine triphosphate.
Who is the labeler?: Apex Energetics Inc., NDC labeler code 63479. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for ENERGY Formula?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.