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NDC 57896-0255-01 Arthritis Pain Relief 650 mg/1 Details
Arthritis Pain Relief 650 mg/1
Arthritis Pain Relief is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by GERI-CARE PHARMACEUTICAL CORP. 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, 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: 57896-0255-01Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Acetaminophen
Product Information
| NDC | 57896-0255 |
|---|---|
| Product ID | 57896-255_f7f77bd4-57c3-148a-e053-6294a90a0f9b |
| 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 | Generic |
| Proprietary Name | Arthritis Pain Relief |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Acetaminophen |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 650 |
| Active Ingredient Units | mg/1 |
| Substance Name | ACETAMINOPHEN |
| Labeler Name | GERI-CARE PHARMACEUTICAL CORP |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA076200 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 57896-0255-01 (57896025501)
| NDC Package Code | 57896-255-01 |
|---|---|
| Billing NDC | 57896025501 |
| Package | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57896-255-01) |
| Marketing Start Date | 2023-03-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |