Magnesium Citrate
- Product NDC
- 0363-0667
- 11-digit product format
- 003630667
- Labeler code
- 0363
- Product ID
- 0363-0667_c77b0a39-d2b8-4e3e-b863-13338a41c789
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Magnesium citrate
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Walgreen Co
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 1989-07-15
- Marketing end
- 0000-00-00
- Substance
- MAGNESIUM CITRATE
- Active strength
- 2 g/29.6mL
- Pharmacologic classes
- Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-0667-38 | 00363066738 | .296 mL in 1 BOTTLE, GLASS (0363-0667-38) | 1989-07-15 | 0000-00-00 | No | No | Current |