Apnetem NDC 75053-0008

NDC codes

FDA NDC Directory

Product NDC (as listed)75053-0008Labeler and product segments. Claims need a package NDC.

Product NDC at billing width75053-0008Add 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
75053-0008-1	75053000801	118 mL in 1 BOTTLE, DROPPER (75053-0008-1)Marketed from May 18, 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): Apnetem
Generic name (nonproprietary): phosphoricum acidum, alumen, phosphorus, senega officinalis, adenosinum cyclophosphoricum, antimonium tartaricum, grindelia, sabadilla, alumina, cuprum metallicum, sanguinarinum nitricum, silicea, lachesis mutus, rheum (palmatum), zincum metallicum, lycopodium clavatum, manganum phosphoricum, antipyrinum, coenzyme a
Active ingredients: Phosphoric acid — 6 [hp_X]/mLPotassium alum — 6 [hp_X]/mLPhosphorus — 9 [hp_X]/mLPolygala senega root — 9 [hp_X]/mLAdenosine cyclic phosphate — 9 [hp_X]/mLAntimony potassium tartrate — 9 [hp_X]/mLGrindelia hirsutula flowering top — 9 [hp_X]/mLSchoenocaulon officinale seed — 9 [hp_X]/mLAluminum oxide — 12 [hp_X]/mLCopper — 12 [hp_X]/mLSanguinarine nitrate — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLRheum palmatum root — 12 [hp_X]/mLZinc — 12 [hp_X]/mLLycopodium clavatum spore — 13 [hp_X]/mLManganese phosphate, Dibasic — 15 [hp_X]/mLAntipyrine — 18 [hp_X]/mLCoenzyme a — 12 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Nucleic Products, LLC
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 18, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Magnetic Resonance Contrast Activity (Mechanism)
Identifiers: Product ID 75053-0008_295ea3ec-7e83-4c0f-bef6-3083376f5913SPL ID 295ea3ec-7e83-4c0f-bef6-3083376f5913SPL set ID ec5bc7e7-4be6-45a6-8cd9-62fdfa7fb469UNII E4GA8884NN, 1L24V9R23S, 27YLU75U4W, M7T6H7D4IF, E0399OZS9N, DL6OZ476V3, IDB0NAZ6AI, 6NAF1689IO, LMI26O6933, 789U1901C5, BOP122S791, ETJ7Z6XBU4, VSW71SS07I, G025DAL7CE, J41CSQ7QDS, C88X29Y479, VZ3U1H7Q5B, T3CHA1B51H, SAA04E81UX
Pharmacologic class: Copper-containing Intrauterine Device; Paramagnetic Contrast Agent

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

N475053000801 followed by a unit qualifier and the quantity

Package 75053-0008-01. 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 14, 2025.

Indications (excerpt from the label)

USES: Temporarily alleviates symptoms of sleep disorders. These "uses" have not been evaluated by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)