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NDC 63629-5284-02 Ibuprofen and Pseudoephedrine hydrochloride 200; 30 mg/1; mg/1 Details

Ibuprofen and Pseudoephedrine hydrochloride 200; 30 mg/1; mg/1

Ibuprofen and Pseudoephedrine hydrochloride is a ORAL TABLET, SUGAR COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Prescription ibuprofen is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). It is also used to relieve mild to moderate pain, including menstrual pain (pain that happens before or during a menstrual period). Nonprescription ibuprofen is used to reduce fever and to relieve minor aches and pain from headaches, muscle aches, arthritis, menstrual periods, the common cold, toothaches, and backaches. Ibuprofen is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.

Related Packages: 63629-5284-02
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Ibuprofen

Pseudoephedrine is used to relieve nasal congestion caused by colds, allergies, and hay fever. It is also used to temporarily relieve sinus congestion and pressure. Pseudoephedrine will relieve symptoms but will not treat the cause of the symptoms or speed recovery. Pseudoephedrine is in a class of medications called nasal decongestants. It works by causing narrowing of the blood vessels in the nasal passages.

Related Packages: 63629-5284-02
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Pseudoephedrine

Product Information

NDC	63629-5284
Product ID	63629-5284_0ea714a1-b05e-bc87-e063-6294a90a28e7
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	Ibuprofen and Pseudoephedrine hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	ibuprofen and pseudoephedrine hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, SUGAR COATED
Route	ORAL
Active Ingredient Strength	200; 30
Active Ingredient Units	mg/1; mg/1
Substance Name	IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
Labeler Name	Bryant Ranch Prepack
Pharmaceutical Class	Adrenergic alpha-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], alpha-Adrenergic Agonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA074567
Listing Certified Through	2025-12-31

Package

NDC 63629-5284-02 (63629528402)

Pricing Information	N/A
NDC Package Code	63629-5284-2
Billing NDC	63629528402
Package	20 TABLET, SUGAR COATED in 1 BOTTLE (63629-5284-2)
Marketing Start Date	2014-03-31
NDC Exclude Flag	N