Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Anpituapar NDC 44911-0526
Sus scrofa pituitary gland 8 [hp_X]/mL + 10 more ingredients · Liquid · Oral · Energique, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 44911-0526-1 | 4491105260144911052601 | 30 mL in 1 BOTTLE, DROPPER (44911-0526-1)Marketed from Feb 25, 2020 |
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)
- Anpituapar
- Generic name (nonproprietary)
- hypophysis suis, agnus castus, baryta carbonica, calcarea carbonica, iodium, natrum muriaticum, phosphoricum acidum, sepia, thyroidinum (suis), lac caninum, adrenocorticotrophin
- Active ingredients
- Sus scrofa pituitary gland — 8 [hp_X]/mLChaste tree fruit — 12 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLIodine — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLThyroid — 12 [hp_X]/mLCanis lupus familiaris milk — 16 [hp_X]/mLCorticotropin — 15 [hp_C]/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
- Listing expires
- Other FDA classes
- Adrenocorticotropic Hormone (Chemical structure)
- Identifiers
- Product ID 44911-0526_8d0fadcd-80ec-4913-b16a-a96e95868588SPL ID 8d0fadcd-80ec-4913-b16a-a96e95868588SPL set ID c0ed2996-8eb5-43f7-b3cc-17477af7f7e9UNII L0PFEMQ1DT, 433OSF3U8A, 6P669D8HQ8, 2E32821G6I, 9679TC07X4, 451W47IQ8X, E4GA8884NN, QDL83WN8C2, 6RV024OAUQ, G39P120JQT, K0U68Q2TXAUPC 0363113700244
- Pharmacologic class
- Adrenocorticotropic 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
N444911052601followed by a unit qualifier and the quantityPackage 44911-0526-01. 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 .
Indications (excerpt from the label)
INDICATIONS: May temporarily relieve weakness, weariness, thirst, PMS, and bone pain.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Excerpt only. Read the full label for complete information.
About NDC 44911-0526
- What is NDC 44911-0526?
- 44911-0526 is the product NDC for Anpituapar, Sus scrofa pituitary gland 8 [hp_X]/mL + 10 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?
- Anpituapar (Hypophysis Suis, Agnus Castus, Baryta Carbonica, Calcarea Carbonica, Iodium, Natrum Muriaticum, Phosphoricum Acidum, Sepia, Thyroidinum (Suis), Lac Caninum, Adrenocorticotrophin).
- What is the active ingredient?
- Sus scrofa pituitary gland, Chaste tree fruit, Barium carbonate, Oyster shell calcium carbonate, Crude, Iodine, Sodium chloride, Phosphoric acid, Sepia officinalis juice, Thyroid, Canis lupus familiaris milk, Corticotropin.
- 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 Anpituapar?
- 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.