Chitoprex
- Product NDC
- 69573-888
- 11-digit product format
- 695730888
- Labeler code
- 69573
- Product ID
- 69573-888_10162a50-f00b-4426-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- 38 Biotech Laboratory LLC
- Dosage form
- CAPSULE
- Route
- DENTAL; INTRAOCULAR; INTRATUMOR; INTRAVENOUS; IRRIGATION; NASAL; ORAL; PERIODONTAL; RECTAL; SUBLINGUAL; TOPICAL; TRANSDERMAL; URETERAL; VAGINAL
- Labeler
- 38 Biotech Laboratory LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-02-27
- Marketing end
- 0000-00-00
- Substance
- CHITOSAN OLIGOSACCHARIDE
- Active strength
- 250 mg/250mg
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 23R93M6Y64 | CHITOSAN OLIGOSACCHARIDE | 9012-76-4 | CHITOSAN OLIGOSACCHARIDE |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Chitoprex | 38 Biotech Laboratory LLC | 2015-02-27 | HUMAN OTC DRUG LABEL | 1 |