acid relief
- Product NDC
- 11822-6123
- 11-digit product format
- 118226123
- Labeler code
- 11822
- Product ID
- 11822-6123_e53e617d-7619-49d4-8e1a-b0f7b3f04288
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA077351
- Marketing category
- ANDA
- Marketing start
- 2023-07-19
- Substance
- FAMOTIDINE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5QZO15J2Z8 | FAMOTIDINE | 76824-35-6 | FAMOTIDINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 11822-6123-0 | 11822612300 | 1 BOTTLE in 1 CARTON (11822-6123-0) / 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2023-07-19 | No | No | Historical |