Search by Drug Name or NDC

NDC 68788-7855-03 Tramadol Hydrochloride and Acetaminophen 325; 37.5 mg/1; mg/1 Details

Tramadol Hydrochloride and Acetaminophen 325; 37.5 mg/1; mg/1

Tramadol Hydrochloride and Acetaminophen is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE.

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: 68788-7855-03
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Acetaminophen

Tramadol is used to relieve moderate to moderately severe pain. Tramadol extended-release tablets and capsules are only used by people who are expected to need medication to relieve pain around-the-clock. Tramadol is in a class of medications called opiate (narcotic) analgesics. It works by changing the way the brain and nervous system respond to pain.

Related Packages: 68788-7855-03
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Tramadol

Product Information

NDC	68788-7855
Product ID	68788-7855_ebb92eef-c6da-45cb-bef8-73ca08fa66db
Associated GPIs	65995002200320
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Tramadol Hydrochloride and Acetaminophen
Proprietary Name Suffix	n/a
Non-Proprietary Name	Tramadol Hydrochloride and Acetaminophen
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	325; 37.5
Active Ingredient Units	mg/1; mg/1
Substance Name	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Labeler Name	Preferred Pharmaceuticals Inc.
Pharmaceutical Class	Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA Schedule	CIV
Marketing Category	ANDA
Application Number	ANDA090485
Listing Certified Through	2024-12-31

Package

NDC 68788-7855-03 (68788785503)

Pricing Information	N/A
NDC Package Code	68788-7855-3
Billing NDC	68788785503
Package	30 TABLET in 1 BOTTLE (68788-7855-3)
Marketing Start Date	2021-01-29
NDC Exclude Flag	N