Package 43598-110-01

Brand: guaifenesin 600 mg

Generic: guaifenesin
NDC Package

Package Facts

Identity

Package NDC 43598-110-01
Digits Only 4359811001
Product NDC 43598-110
Product ID 43598-110_ef6a6eb4-cde7-cd56-0290-29d56beec22c
Description

5 BLISTER PACK in 1 CARTON (43598-110-01) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-09-01
Brand guaifenesin 600 mg
Generic guaifenesin
Sample Package No

Linked Drug Pages (1)

Guaifenesin 1200 mg, Guaifenesin 600 mg ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ef6a6eb4-cde7-cd56-0290-29d56beec22c", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310621", "636522"], "spl_set_id": ["525fda90-134c-f038-c403-eb5ffc1fb1f1"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "5 BLISTER PACK in 1 CARTON (43598-110-01)  / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "43598-110-01", "marketing_start_date": "20220901"}], "brand_name": "Guaifenesin 600 mg", "product_id": "43598-110_ef6a6eb4-cde7-cd56-0290-29d56beec22c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "43598-110", "generic_name": "Guaifenesin", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin 600 mg", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA215932", "marketing_category": "ANDA", "marketing_start_date": "20220901", "listing_expiration_date": "20261231"}