What is NDC 44911-0278?

44911-0278 is the product NDC for Postpituapar, Apis mellifera 12 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Postpituapar (Apis Mellifica, Arsenicum Album, Lachesis Mutus, Nux Vomica, Phosphoricum Acidum, Pituitarum Posterium (Bovine), Pulsatilla (Pratensis), Sambucus Nigra, Thuja Occidentalis).

What is the active ingredient?

Apis mellifera, Arsenic trioxide, Lachesis muta venom, Strychnos nux-vomica seed, Phosphoric acid, Bos taurus pituitary gland, Posterior, Pulsatilla pratensis whole, Sambucus nigra flowering top, Thuja occidentalis leafy twig.

Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Postpituapar?

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.

Postpituapar NDC 44911-0278 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0278Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0278Add 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
44911-0278-1	4491102780144911027801	30 mL in 1 BOTTLE, DROPPER (44911-0278-1)Marketed from Oct 1, 2015

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): Postpituapar
Generic name (nonproprietary): apis mellifica, arsenicum album, lachesis mutus, nux vomica, phosphoricum acidum, pituitarum posterium (bovine), pulsatilla (pratensis), sambucus nigra, thuja occidentalis
Active ingredients: Apis mellifera — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLBos taurus pituitary gland, Posterior — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLSambucus nigra flowering top — 12 [hp_X]/mLThuja occidentalis leafy twig — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.NDC labeler code 44911
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 1, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 44911-0278_b6b5ad58-404f-4376-a745-0fa897c5d064SPL ID b6b5ad58-404f-4376-a745-0fa897c5d064SPL set ID 1212410f-ebe9-40b8-85f6-27bd45456e4aUNII 7S82P3R43Z, S7V92P67HO, VSW71SS07I, 269XH13919, E4GA8884NN, 7JM57I419K, 8E272251DI, CT03BSA18U, 1NT28V9397UPC 0363113700138
Pharmacologic class: Non-Standardized Plant Allergenic Extract; Standardized Insect Venom 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

N444911027801 followed by a unit qualifier and the quantity

Package 44911-0278-01. 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 Oct 29, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve weakness, lethargy and frequent urination.** 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 44911-0278

What is NDC 44911-0278?: 44911-0278 is the product NDC for Postpituapar, Apis mellifera 12 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Postpituapar (Apis Mellifica, Arsenicum Album, Lachesis Mutus, Nux Vomica, Phosphoricum Acidum, Pituitarum Posterium (Bovine), Pulsatilla (Pratensis), Sambucus Nigra, Thuja Occidentalis).
What is the active ingredient?: Apis mellifera, Arsenic trioxide, Lachesis muta venom, Strychnos nux-vomica seed, Phosphoric acid, Bos taurus pituitary gland, Posterior, Pulsatilla pratensis whole, Sambucus nigra flowering top, Thuja occidentalis leafy twig.
Who is the labeler?: Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Postpituapar?: 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.