Curist Acid Relief
- Product NDC
- 72559-032
- 11-digit product format
- 725590032
- Labeler code
- 72559
- Product ID
- 72559-032_4c2614fe-f789-8512-e063-6394a90a22cf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine 20 mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Little Pharma, Inc.
- Application
- ANDA215822
- Marketing category
- ANDA
- Marketing start
- 2024-01-31
- 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
- Curist Acid Relief
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FAMOTIDINE | 20 mg/1 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72559-032-23 | Curist Acid Relief | 300 in 1 BOTTLE | TABLET | 300 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72559-032 | CURIST ACID RELIEF (FAMOTIDINE 20 MG) TABLET [LITTLE PHARMA, INC.] | 1 | Current NDC, 1 package rows | 20240201_0fdfcc7c-aeed-6bd0-e063-6394a90ae52d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72559-032-23 | 72559003223 | 300 TABLET in 1 BOTTLE (72559-032-23) | 300 tablet | 2024-01-31 | No | No | Historical |