Pituistat NDC 44911-0266

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0266Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0266Add 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
44911-0266-1	44911026601	50 mL in 1 PACKAGE (44911-0266-1)Marketed from Sep 24, 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): Pituistat
Generic name (nonproprietary): aralia quinquefolia, ginkgo biloba, arsenicum iodatum, avena sativa, baryta carbonica, phosphorus, silicea, thyroidinum (suis), aluminum, antimony, barium, beryllium, bismuth, boron, bromine, calcium, carbon, cerium, cesium, chloride, chromium, cobalt, copper, dysprosium, erbium, europium, fluoride, gadolinium, gallium, germanium, gold, hafnium, holmium, indium, iodine, iridium, iron, lanthanum, lithium, lutetium, magnesium, manganese, molybdenum, neodymium, nickel, niobium, osmium, palladium
Active ingredients: American ginseng — 3 [hp_X]/mLGinkgo — 3 [hp_X]/mLArsenic triiodide — 12 [hp_X]/mLAvena sativa flowering top — 12 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLThyroid — 12 [hp_X]/mLAluminum — 12 [hp_X]/mLAntimony — 12 [hp_X]/mLBarium — 12 [hp_X]/mLBeryllium — 12 [hp_X]/mLBismuth — 12 [hp_X]/mLBoron — 12 [hp_X]/mLBromine — 12 [hp_X]/mLCalcium — 12 [hp_X]/mLActivated charcoal — 12 [hp_X]/mLCerium — 12 [hp_X]/mLCesium — 12 [hp_X]/mLChloride ion — 12 [hp_X]/mLChromium — 12 [hp_X]/mLCobalt — 12 [hp_X]/mLCopper — 12 [hp_X]/mLDysprosium — 12 [hp_X]/mLErbium — 12 [hp_X]/mLEuropium — 12 [hp_X]/mLFluoride ion — 12 [hp_X]/mLGadolinium — 12 [hp_X]/mLGallium — 12 [hp_X]/mLGermanium — 12 [hp_X]/mLGold — 12 [hp_X]/mLHafnium — 12 [hp_X]/mLHolmium — 12 [hp_X]/mLIndium — 12 [hp_X]/mLIodine — 12 [hp_X]/mLIridium — 12 [hp_X]/mLIron — 12 [hp_X]/mLLanthanum — 12 [hp_X]/mLLithium — 12 [hp_X]/mLLutetium — 12 [hp_X]/mLMagnesium — 12 [hp_X]/mLManganese — 12 [hp_X]/mLMolybdenum — 12 [hp_X]/mLNeodymium — 12 [hp_X]/mLNickel — 12 [hp_X]/mLNiobium — 12 [hp_X]/mLOsmium — 12 [hp_X]/mLPalladium — 12 [hp_X]/mLPlatinum — 12 [hp_X]/mLPotassium — 12 [hp_X]/mLPraseodymium — 12 [hp_X]/mLRhenium — 12 [hp_X]/mLRhodium — 12 [hp_X]/mLRubidium — 12 [hp_X]/mLRuthenium — 12 [hp_X]/mLSamarium — 12 [hp_X]/mLScandium — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLSilicon — 12 [hp_X]/mLSilver — 12 [hp_X]/mLSodium — 12 [hp_X]/mLStrontium — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLTantalum — 12 [hp_X]/mLTellurium — 12 [hp_X]/mLTerbium — 12 [hp_X]/mLThallium — 12 [hp_X]/mLThorium — 12 [hp_X]/mLThulium — 12 [hp_X]/mLTin — 12 [hp_X]/mLTitanium — 12 [hp_X]/mLTungsten — 12 [hp_X]/mLVanadium — 12 [hp_X]/mLYtterbium — 12 [hp_X]/mLYttrium — 12 [hp_X]/mLZinc — 12 [hp_X]/mLZirconium — 12 [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, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Calcium (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 44911-0266_630ce8b7-1624-47f7-8fc9-6026e66a9ac1SPL ID 630ce8b7-1624-47f7-8fc9-6026e66a9ac1SPL set ID 27a5fccb-8707-4bb5-a848-d1921bba2f7fUNII 8W75VCV53Q, 19FUJ2C58T, 3029988O2T, MA9CQJ3F7F, 6P669D8HQ8, 27YLU75U4W, ETJ7Z6XBU4, 6RV024OAUQ, CPD4NFA903, 9IT35J3UV3, 24GP945V5T, OW5102UV6N, U015TT5I8H, N9E3X5056Q, SBV4XY874G, SY7Q814VUP, 2P3VWU3H10, 30K4522N6T, 1KSV9V4Y4I, Q32ZN48698, 0R0008Q3JB, 3G0H8C9362, 789U1901C5, 1D4N45714Q, 77B218D3YE, 444W947O8O, Q80VPU408O, AU0V1LM3JT, CH46OC8YV4, 00072J7XWS, 79Y1949PYO, X71938L1DO, W1XX32SQN1, 045A6V3VFX, 9679TC07X4, 44448S9773, E1UOL152H7, 6I3K30563S, 9FN79X2M3F, 5H0DOZ21UJ, I38ZP9992A, 42Z2K6ZL8P, 81AH48963U, 2I87U3734A, 7OV03QG267, 05175J654G, 2E7M255OPY, 5TWQ1V240M, 49DFR088MY, RWP5GA015D, NKN7EZA750, 7YHU292INY, DMK383DSAC, MLT4718TJW, 7UI0TKC3U5, 42OD65L39F, YUJ4U1EW7R, H6241UJ22B, Z4152N8IUI, 3M4G523W1G, 9NEZ333N27, YZS2RPE8LE, 70FD1KFU70, 6424HBN274, NQA0O090ZJ, 06SSF7P179, AD84R52XLF, 60YU5MIG9W, 8RKC5ATI4P, 387GMG9FH5, D1JT611TNE, V9306CXO6G, 00J9J9XKDE, MNQ4O4WSI1, 58784XQC3Y, J41CSQ7QDS, C6V6S92N3CUPC 0363113700763
Pharmacologic class: Calcium; Copper-containing Intrauterine Device; Mood Stabilizer; Standardized Chemical Allergen

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

N444911026601 followed by a unit qualifier and the quantity

Package 44911-0266-01. 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 21, 2023.

Indications (excerpt from the label)

INDICATIONS: For temporarily relieve mental sluggishness, confusion, weakness, lethargy, thirst, and frequent urination. **Claims based upon 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)