- Product NDC
- 11673-010
- 11-digit product format
- 116730010
- Labeler code
- 11673
- Product ID
- 11673-010_467d1aa6-b363-4314-9806-e4f4a495bdab
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine, Calcium Carbonate, Magnesium Hydroxide
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA077355
- Marketing category
- ANDA
- Marketing start
- 2015-05-06
- Marketing end
- 0000-00-00
- Substance
- CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE
- Active strength
- 800 mg/1; mg/1; mg/1
- Pharmacologic classes
- Calculi Dissolution Agent [EPC], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [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