Pain Reliever
- Product NDC
- 50844-255
- 11-digit product format
- 508440255
- Labeler code
- 50844
- Product ID
- 50844-255_cb980327-4973-491f-904d-1193ef3a51ec
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- L.N.K. International, Inc.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-07-23
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pain Reliever
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50844-255-08 | Pain Reliever | 24 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 24 | | 8 |
| 50844-255-08 | Pain Reliever | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50844-255 | PAIN RELIEVER (ACETAMINOPHEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] | 7 | Current NDC, Legacy NDC, 2 package rows | 20241027_734cc3d2-6fc5-4dcc-93ed-0b57c1f01345.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 |
|---|
| 50844-255-08 | 50844025508 | 1 BOTTLE, PLASTIC in 1 CARTON (50844-255-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2019-07-23 | 0000-00-00 | No | No | Current |