Pain Reliever
- Product NDC
- 49580-2880
- 11-digit product format
- 495802880
- Labeler code
- 49580
- Product ID
- 49580-2880_7dfcadc9-97a1-4d12-b8d9-2053c4ee9273
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-03-15
- Marketing end
- 2026-12-30
- Substance
- ACETAMINOPHEN
- Active strength
- 160 mg/5mL
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pain Reliever
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 160 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 307668 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49580-2880-4 | Pain Reliever | 1 in 1 BOX | SUSPENSION | 1 | | 4 |
| 49580-2880-4 | Pain Reliever | 118 mL in 1 BOTTLE, PLASTIC | SUSPENSION | 118 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49580-2880 | PAIN RELIEVER (ACETAMINOPHEN) SUSPENSION [P & L DEVELOPMENT, LLC] | 3 | Current NDC, 2 package rows | 20240316_64c642b7-ef83-44b7-a014-6fa248dff3ba.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49580-2880-4 | 49580288004 | 1 BOTTLE, PLASTIC in 1 BOX (49580-2880-4) / 118 mL in 1 BOTTLE, PLASTIC | 2024-03-15 | 2026-12-30 | No | No | Historical |