Anpituapar
- Product NDC
- 44911-0049
- 11-digit product format
- 449110049
- Labeler code
- 44911
- Product ID
- 44911-0049_caf6c824-a7a5-4710-a4ec-406c60e4519e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Adrenocorticotrophin, Agnus Castus, Baryta Castus, Baryta Carbonica, Calcarea Carbonica, Iodium, Lac Caninum, Natrum Muriaticum, Phosphoricum Acidum, Sepia, Thyroidinum (Suis)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-10-29
- Marketing end
- 2020-07-22
- Substance
- CORTICOTROPIN; CHASTE TREE; BARIUM CARBONATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; IODINE; CANIS LUPUS FAMILIARIS MILK; SODIUM CHLORIDE; PHOSPHORIC ACID; SEPIA OFFICINALIS JUICE; SUS SCROFA THYROID
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Adrenocorticotropic Hormone [CS],Adrenocorticotropic Hormone [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record