Hevert Gelsemium comp
- Product NDC
- 54532-0027
- 11-digit product format
- 545320027
- Labeler code
- 54532
- Product ID
- 54532-0027_ddd6316e-3775-4858-9e7f-fbb4b0a6f261
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- aconitum napellus, anamirta cocculus seed, citrullus colocynthis fruit, gelsemium sempervirens root, lachesis muta venom, daphne mezereum bark, strychnos nux-vomica seed, lead acetate anhydrous, and toxicodendron pubescens shoot
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Hevert Pharmaceuticals LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-06-01
- Marketing end
- 2021-12-31
- Substance
- ACONITUM NAPELLUS WHOLE; ANAMIRTA COCCULUS SEED; CITRULLUS COLOCYNTHIS FRUIT; GELSEMIUM SEMPERVIRENS ROOT; LACHESIS MUTA VENOM; DAPHNE MEZEREUM BARK; STRYCHNOS NUX-VOMICA SEED; LEAD ACETATE ANHYDROUS; TOXICODENDRON PUBESCENS SHOOT
- Active strength
- 4 [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL
- Pharmacologic classes
- Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Plant Proteins [CS],Seed Storage Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 54532-0027-4 | 54532002704 | 10 AMPULE in 1 CARTON (54532-0027-4) > 2 mL in 1 AMPULE | 10 ampule | 2016-06-01 | 0000-00-00 | No | No | Current |