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NDC 41163-0520-01 Acetaminophen Gelcaps 500 mg/1 Details
Acetaminophen Gelcaps 500 mg/1
Acetaminophen Gelcaps is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by United Natural Foods, Inc. dba UNFI. 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: 41163-0520-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Acetaminophen
Product Information
| NDC | 41163-0520 |
|---|---|
| Product ID | 41163-520_fbe573b2-eb1d-af53-e053-6394a90a2dc9 |
| Associated GPIs | 64200010000315 |
| GCN Sequence Number | 004490 |
| GCN Sequence Number Description | acetaminophen TABLET 500 MG ORAL |
| HIC3 | H3E |
| HIC3 Description | ANALGESIC/ANTIPYRETICS,NON-SALICYLATE |
| GCN | 16965 |
| HICL Sequence Number | 001866 |
| HICL Sequence Number Description | ACETAMINOPHEN |
| Brand/Generic | Generic |
| Proprietary Name | Acetaminophen Gelcaps |
| Proprietary Name Suffix | Extra Strength |
| Non-Proprietary Name | Acetaminophen |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, COATED |
| Route | ORAL |
| Active Ingredient Strength | 500 |
| Active Ingredient Units | mg/1 |
| Substance Name | ACETAMINOPHEN |
| Labeler Name | United Natural Foods, Inc. dba UNFI |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 41163-0520-01 (41163052001)
| NDC Package Code | 41163-520-01 |
|---|---|
| Billing NDC | 41163052001 |
| Package | 1 BOTTLE, PLASTIC in 1 CARTON (41163-520-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC |
| Marketing Start Date | 2014-11-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |