Search by Drug Name or NDC

NDC 72865-0203-01 Hydrocodone Bitartrate and Acetaminophen 325; 7.5 mg/1; mg/1 Details

Hydrocodone Bitartrate and Acetaminophen 325; 7.5 mg/1; mg/1

Hydrocodone Bitartrate and Acetaminophen is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by XLCare Pharmaceuticals, Inc.. The primary component is ACETAMINOPHEN; HYDROCODONE BITARTRATE.

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: 72865-0203-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Acetaminophen

Hydrocodone is available in combination with other ingredients, and different combination products are prescribed for different uses. Some hydrocodone combination products are used to relieve moderate-to-severe pain. Other hydrocodone combination products are used to relieve cough. Hydrocodone is in a class of medications called opiate (narcotic) analgesics and in a class of medications called antitussives. Hydrocodone relieves pain by changing the way the brain and nervous system respond to pain. Hydrocodone relieves cough by decreasing activity in the part of the brain that causes coughing. You will take hydrocodone in combination with at least one other medication, but this monograph only provides information about hydrocodone. Be sure to read information about the other ingredients in the hydrocodone product you are taking. Ask your doctor or pharmacist if you have any questions.

Related Packages: 72865-0203-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Hydrocodone Combination Products

Product Information

NDC	72865-0203
Product ID	72865-203_4533550e-d20a-4329-b5ab-fb7542ce0be9
Associated GPIs
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	Hydrocodone Bitartrate and Acetaminophen
Proprietary Name Suffix	n/a
Non-Proprietary Name	Hydrocodone Bitartrate and Acetaminophen
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	325; 7.5
Active Ingredient Units	mg/1; mg/1
Substance Name	ACETAMINOPHEN; HYDROCODONE BITARTRATE
Labeler Name	XLCare Pharmaceuticals, Inc.
Pharmaceutical Class	Opioid Agonist [EPC], Opioid Agonists [MoA]
DEA Schedule	CII
Marketing Category	ANDA
Application Number	ANDA211487
Listing Certified Through	2024-12-31

Package

NDC 72865-0203-01 (72865020301)

Pricing Information	N/A
NDC Package Code	72865-203-01
Billing NDC	72865020301
Package	100 TABLET in 1 BOTTLE (72865-203-01)
Marketing Start Date	2020-02-27
NDC Exclude Flag	N