Endoplex M
- Product NDC
- 43857-0280
- 11-digit product format
- 438570280
- Labeler code
- 43857
- Product ID
- 43857-0280_390cbe33-8af3-4da8-8b3a-902cc2d68c60
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Agnus Castus, Aralia Quinquefolia, Juniperus Virginiana, Lycopodium Clavatum, Petroselinum Sativum, Pulsatilla (Vulgaris), Sabal Serrulata, Urtica Dioica, Xanthoxylum Fraxineum, Glandula Suprarenalis Suis, Orchitinum (Suis), Pituitaria Glandula (suis), Prostate (suis), Clematis Erecta
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-08-15
- Marketing end
- 2022-01-15
- Substance
- CHASTE TREE; AMERICAN GINSENG; JUNIPERUS VIRGINIANA TWIG; LYCOPODIUM CLAVATUM SPORE; PETROSELINUM CRISPUM; PULSATILLA VULGARIS; SAW PALMETTO; URTICA DIOICA; ZANTHOXYLUM AMERICANUM BARK; SUS SCROFA ADRENAL GLAND; SUS SCROFA TESTICLE; SUS SCROFA PITUITARY GLAND; SUS SCROFA PROSTATE; CLEMATIS RECTA FLOWERING TOP
- Active strength
- 3 [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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43857-0280-1 | 43857028001 | 30 mL in 1 BOTTLE, DROPPER (43857-0280-1) | 30 ml | 2014-08-15 | 2022-01-15 | No | No | Current |