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NDC 68788-7763-03 TRAMADOL HYDROCHLORIDE 100 mg/1 Details

TRAMADOL HYDROCHLORIDE 100 mg/1

TRAMADOL HYDROCHLORIDE is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is TRAMADOL HYDROCHLORIDE.

MedlinePlus Drug Summary

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: 68788-7763-03
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Tramadol

Product Information

NDC	68788-7763
Product ID	68788-7763_2980e491-7b1c-460b-a96a-ae5862c35300
Associated GPIs	65100095107520
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
Proprietary Name Suffix	n/a
Non-Proprietary Name	TRAMADOL HYDROCHLORIDE
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	100
Active Ingredient Units	mg/1
Substance Name	TRAMADOL HYDROCHLORIDE
Labeler Name	Preferred Pharmaceuticals, Inc.
Pharmaceutical Class	Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA Schedule	CIV
Marketing Category	ANDA
Application Number	ANDA201384
Listing Certified Through	2024-12-31

Package

NDC 68788-7763-03 (68788776303)

Pricing Information	N/A
NDC Package Code	68788-7763-3
Billing NDC	68788776303
Package	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7763-3)
Marketing Start Date	2020-07-22
NDC Exclude Flag	N