guaifenesin and dextromethorphan hbr
Generic: guaifenesin and dextromethorphan hbr
Labeler: aurohealth llcDrug Facts
Product Profile
Brand Name
guaifenesin and dextromethorphan hbr
Generic Name
guaifenesin and dextromethorphan hbr
Labeler
aurohealth llc
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
dextromethorphan hydrobromide 30 mg/1, guaifenesin 600 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
58602-714
Product ID
58602-714_cfc45418-1bd2-4f68-b1c9-ed3f2bc006aa
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA206941
Listing Expiration
2026-12-31
Marketing Start
2017-03-17
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
58602714
Hyphenated Format
58602-714
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
guaifenesin and dextromethorphan hbr (source: ndc)
Generic Name
guaifenesin and dextromethorphan hbr (source: ndc)
Application Number
ANDA206941 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
- 600 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (58602-714-05) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
- 6 BLISTER PACK in 1 CARTON (58602-714-07) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (58602-714-03)
- 4 BLISTER PACK in 1 CARTON (58602-714-08) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (58602-714-03)
- 1 BOTTLE in 1 CARTON (58602-714-09) / 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (58602-714-12) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (58602-714-15) / 60 TABLET, EXTENDED RELEASE in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (58602-714-66) / 58 TABLET, EXTENDED RELEASE in 1 BOTTLE
- 2 BLISTER PACK in 1 CARTON (58602-714-67) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (58602-714-03)
- 1 BOTTLE in 1 CARTON (58602-714-73) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE
Packages (9)
58602-714-05
1 BOTTLE in 1 CARTON (58602-714-05) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
58602-714-07
6 BLISTER PACK in 1 CARTON (58602-714-07) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (58602-714-03)
58602-714-08
4 BLISTER PACK in 1 CARTON (58602-714-08) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (58602-714-03)
58602-714-09
1 BOTTLE in 1 CARTON (58602-714-09) / 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
58602-714-12
1 BOTTLE in 1 CARTON (58602-714-12) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE
58602-714-15
1 BOTTLE in 1 CARTON (58602-714-15) / 60 TABLET, EXTENDED RELEASE in 1 BOTTLE
58602-714-66
1 BOTTLE in 1 CARTON (58602-714-66) / 58 TABLET, EXTENDED RELEASE in 1 BOTTLE
58602-714-67
2 BLISTER PACK in 1 CARTON (58602-714-67) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (58602-714-03)
58602-714-73
1 BOTTLE in 1 CARTON (58602-714-73) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cfc45418-1bd2-4f68-b1c9-ed3f2bc006aa", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["cc20129b-2556-4452-9222-afd503f1e7a4"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-714-05) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-714-05", "marketing_start_date": "20170317"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (58602-714-07) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (58602-714-03)", "package_ndc": "58602-714-07", "marketing_start_date": "20170317"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (58602-714-08) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (58602-714-03)", "package_ndc": "58602-714-08", "marketing_start_date": "20170317"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-714-09) / 30 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-714-09", "marketing_start_date": "20170317"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-714-12) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-714-12", "marketing_start_date": "20170317"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-714-15) / 60 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-714-15", "marketing_start_date": "20170317"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-714-66) / 58 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-714-66", "marketing_start_date": "20170317"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (58602-714-67) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (58602-714-03)", "package_ndc": "58602-714-67", "marketing_start_date": "20170317"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-714-73) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-714-73", "marketing_start_date": "20170317"}], "brand_name": "Guaifenesin and Dextromethorphan HBr", "product_id": "58602-714_cfc45418-1bd2-4f68-b1c9-ed3f2bc006aa", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "58602-714", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin and Dextromethorphan HBr", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}, {"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA206941", "marketing_category": "ANDA", "marketing_start_date": "20170317", "listing_expiration_date": "20261231"}