Up and Up Dual Action Acid Reducer and Antacid
- Product NDC
- 82442-546
- 11-digit product format
- 824420546
- Labeler code
- 82442
- Product ID
- 82442-546_2ce787d5-a3e1-4202-a051-e15771441812
- 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
- 2025-09-02
- Substance
- CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE
- Active strength
- 800; 10; 165 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Up and Up Dual Action Acid Reducer and Antacid
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCIUM CARBONATE | 800 mg/1 |
| FAMOTIDINE | 10 mg/1 |
| MAGNESIUM HYDROXIDE | 165 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | H0G9379FGK, 5QZO15J2Z8, NBZ3QY004S |
| Rxcui | 283641 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82442-546-71 | 82442054671 | 50 TABLET, CHEWABLE in 1 BOTTLE (82442-546-71) | 2025-09-02 | No | No | Historical |