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NDC 50580-0783-10 Tylenol 8 HR Arthritis Pain 650 mg/1 Details
Tylenol 8 HR Arthritis Pain 650 mg/1
Tylenol 8 HR Arthritis Pain is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Johnson & Johnson Consumer Inc.. The primary component is ACETAMINOPHEN.
MedlinePlus Drug Summary
Acetaminophen is used to relieve mild to moderate pain from headaches, muscle aches, menstrual periods, colds and sore throats, toothaches, backaches, and reactions to vaccinations (shots), and to reduce fever. Acetaminophen may also be used to relieve the pain of osteoarthritis (arthritis caused by the breakdown of the lining of the joints). Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.
Related Packages: 50580-0783-10Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Acetaminophen
Product Information
| NDC | 50580-0783 |
|---|---|
| Product ID | 50580-783_f79f902f-03d2-7558-e053-6394a90a3a43 |
| Associated GPIs | |
| GCN Sequence Number | 022123 |
| GCN Sequence Number Description | acetaminophen TABLET ER 650 MG ORAL |
| HIC3 | H3E |
| HIC3 Description | ANALGESIC/ANTIPYRETICS,NON-SALICYLATE |
| GCN | 16910 |
| HICL Sequence Number | 001866 |
| HICL Sequence Number Description | ACETAMINOPHEN |
| Brand/Generic | Brand |
| Proprietary Name | Tylenol 8 HR Arthritis Pain |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Acetaminophen |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 650 |
| Active Ingredient Units | mg/1 |
| Substance Name | ACETAMINOPHEN |
| Labeler Name | Johnson & Johnson Consumer Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA019872 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50580-0783-10 (50580078310)
| NDC Package Code | 50580-783-10 |
|---|---|
| Billing NDC | 50580078310 |
| Package | 1 BOTTLE, PLASTIC in 1 CARTON (50580-783-10) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
| Marketing Start Date | 2015-07-13 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |