acid controller
- Product NDC
- 21130-521
- 11-digit product format
- 211300521
- Labeler code
- 21130
- Product ID
- 21130-521_2e7c8340-ff76-4d41-bda4-e47fd0f7e10a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Safeway
- Application
- ANDA077351
- Marketing category
- ANDA
- Marketing start
- 2025-06-27
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- acid controller
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FAMOTIDINE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5QZO15J2Z8 |
| Rxcui | 310273 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21130-521-82 | acid controller | 200 in 1 BOTTLE | TABLET, FILM COATED | 200 | | 2 |
| 21130-521-82 | acid controller | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 21130-521-82 | 21130052182 | 1 BOTTLE in 1 CARTON (21130-521-82) / 200 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2025-06-27 | No | No | Current |