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
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69573-888-11 | Chitoprex101 | 500 mg in 1 CAPSULE | CAPSULE | 500 | | 1 |
| 69573-888-33 | Chitoprex101 | 30 in 1 BOTTLE | CAPSULE | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69573-888 | CHITOPREX 101 (38 BIOTECH LABORATORY LLC) CAPSULE [38 BIOTECH LABORATORY LLC] | 1 | Legacy NDC, 2 package rows | 20150618_10162a50-f00a-4426-e054-00144ff88e88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 69573-888-11 | 69573088811 | 500 mg in 1 CAPSULE | 500 mg | Historical |
| 69573-888-33 | 69573088833 | 30 in 1 BOTTLE | | Historical |