guaifenesin and dextromethorphan hydrobromide hbr
Generic: guaifenesin and dextromethorphan hydrobromide
Labeler: rite-aidDrug Facts
Product Profile
Brand Name
guaifenesin and dextromethorphan hydrobromide hbr
Generic Name
guaifenesin and dextromethorphan hydrobromide
Labeler
rite-aid
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
dextromethorphan hydrobromide 60 mg/1, guaifenesin 1200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
11822-9996
Product ID
11822-9996_3b1ee432-8657-4ef6-9b89-cf0127157e64
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA214781
Listing Expiration
2026-12-31
Marketing Start
2022-06-28
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
118229996
Hyphenated Format
11822-9996
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 hydrobromide hbr (source: ndc)
Generic Name
guaifenesin and dextromethorphan hydrobromide (source: ndc)
Application Number
ANDA214781 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 60 mg/1
- 1200 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (11822-9996-1) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
- 2 BLISTER PACK in 1 CARTON (11822-9996-2) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b1ee432-8657-4ef6-9b89-cf0127157e64", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["2343f031-d658-498a-b5d1-6dcdb26b3cf0"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["RITE-AID"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (11822-9996-1) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "11822-9996-1", "marketing_start_date": "20220628"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (11822-9996-2) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "11822-9996-2", "marketing_start_date": "20220628"}], "brand_name": "Guaifenesin and Dextromethorphan Hydrobromide HBR", "product_id": "11822-9996_3b1ee432-8657-4ef6-9b89-cf0127157e64", "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": "11822-9996", "generic_name": "guaifenesin and dextromethorphan hydrobromide", "labeler_name": "RITE-AID", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin and Dextromethorphan Hydrobromide HBR", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA214781", "marketing_category": "ANDA", "marketing_start_date": "20220628", "listing_expiration_date": "20261231"}