ACID REDUCER
- Product NDC
- 56062-088
- 11-digit product format
- 560620088
- Labeler code
- 56062
- Product ID
- 56062-088_b3862f03-3efe-4e65-a637-46441e9ab01f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Publix Super Markets Inc
- Application
- ANDA077351
- Marketing category
- ANDA
- Marketing start
- 2026-03-06
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ACID REDUCER
- Listing expiration
- 2027-12-31
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 |
|---|
| 56062-088-02 | ACID REDUCER | 25 in 1 CARTON | TABLET, FILM COATED | 25 | | 2 |
| 56062-088-02 | ACID REDUCER | 1 in 1 BLISTER PACK | 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 |
|---|
| 56062-088-02 | 56062008802 | 25 BLISTER PACK in 1 CARTON (56062-088-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK | 25 blister pack | 2026-03-06 | No | No | Historical |