Arthritis Pain Relief
- Product NDC
- 67091-401
- 11-digit product format
- 670910401
- Labeler code
- 67091
- Product ID
- 67091-401_f9159d83-e662-0576-e053-6394a90a651a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- WINCO FOODS, LLC
- Application
- ANDA211544
- Marketing category
- ANDA
- Marketing start
- 2023-04-11
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 362O9ITL9D | ACETAMINOPHEN | 103-90-2 | ACETAMINOPHEN |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 67091-401-02 | 67091040102 | 2 BOTTLE, PLASTIC in 1 CARTON (67091-401-02) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC | 2023-04-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| 1200A-WNC-2023-0411 | WINCO FOODS, LLC | 2023-04-11 | HUMAN OTC DRUG LABEL | 2 |