ACID CONTROLLER
- Product NDC
- 21130-771
- 11-digit product format
- 211300771
- Labeler code
- 21130
- Product ID
- 21130-771_cafa4061-7e52-4374-9f4b-4a01ff6e4c07
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Safeway
- Application
- ANDA075400
- Marketing category
- ANDA
- Marketing start
- 2025-08-13
- Substance
- FAMOTIDINE
- Active strength
- 10 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 |
|---|
| 21130-771-75 | 21130077175 | 1 BOTTLE in 1 CARTON (21130-771-75) / 90 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2025-08-13 | No | No | Historical |