FeverAll
- Product NDC
- 51672-5319
- 11-digit product format
- 516725319
- Labeler code
- 51672
- Product ID
- 51672-5319_38f91f45-9b1c-befa-e063-6294a90a3cc1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-06-01
- Substance
- ACETAMINOPHEN
- Active strength
- 160 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FeverAll
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 160 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 307668, 2639351 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51672-5319-8 | FeverAll | 1 in 1 CARTON | SUSPENSION | 1 | | 4 |
| 51672-5319-8 | FeverAll | 118 mL in 1 BOTTLE | SUSPENSION | 118 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51672-5319 | FEVERALL (ACETAMINOPHEN) SUSPENSION [TARO PHARMACEUTICALS U.S.A., INC.] | 3 | Current NDC, 2 package rows | 20241115_8970b91b-5f3c-4764-9e23-25dcb398d0a7.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 |
|---|
| 51672-5319-8 | 51672531908 | 1 BOTTLE in 1 CARTON (51672-5319-8) / 118 mL in 1 BOTTLE | 1 bottle | 2023-06-01 | No | No | Historical |