United States · FDA National Drug Code directory
Hypothalmupar
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 44911-0473_e646941c-406d-4e3e-af16-bcd09d44ea78
- Product NDC
- 44911-0473
- Form
- LIQUID
- Composition / generic term
- Aralia Quinquefolia, Ginkgo Biloba, Hydrocotyle Asiatica, Cerebrum Suis, Hypophysis Suis, Hypothalamus Suis, Phosphorus, Silicea
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20180924
- Source listing expiry
- 20261231
Source-listed ingredients
- AMERICAN GINSENG — 3 [hp_X]/mL
- GINKGO — 3 [hp_X]/mL
- CENTELLA ASIATICA WHOLE — 3 [hp_X]/mL
- SUS SCROFA CEREBRUM — 8 [hp_X]/mL
- SUS SCROFA PITUITARY GLAND — 8 [hp_X]/mL
- SUS SCROFA HYPOTHALAMUS — 12 [hp_X]/mL
- PHOSPHORUS — 12 [hp_X]/mL
- SILICON DIOXIDE — 12 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 mL in 1 BOTTLE, DROPPER (44911-0473-1) · 44911-0473-1
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →