Herplex
- Product NDC
- 49744-0001
- 11-digit product format
- 497440001
- Labeler code
- 49744
- Product ID
- 49744-0001_e673de3f-7483-4b80-955a-7ffda9a12935
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Anatherum Muricatum, Clematis Erecta, Mezereum, Phytolacca Decandra, Ranunculus Bulbosus, Rhus Tox, Thuja Occidentalis, Natrum Muriaticum, Sepia
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Paradigm, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-07-22
- Marketing end
- 2023-04-19
- Substance
- CHRYSOPOGON ZIZANIOIDES ROOT; CLEMATIS RECTA FLOWERING TOP; DAPHNE MEZEREUM BARK; PHYTOLACCA AMERICANA ROOT; RANUNCULUS BULBOSUS; TOXICODENDRON PUBESCENS LEAF; THUJA OCCIDENTALIS LEAFY TWIG; SODIUM CHLORIDE; SEPIA OFFICINALIS JUICE
- Active strength
- 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- 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 |
|---|
| 49744-0001-1 | 49744000101 | 60 TABLET in 1 BOTTLE (49744-0001-1) | 60 tablet | 2016-09-27 | 2023-04-19 | No | No | Current |