cough dm
Generic: dextromethorphan polistirex
Labeler: h e bDrug Facts
Product Profile
Brand Name
cough dm
Generic Name
dextromethorphan polistirex
Labeler
h e b
Dosage Form
SUSPENSION
Routes
Active Ingredients
dextromethorphan hydrobromide 30 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
37808-384
Product ID
37808-384_76f9d0f8-2bb8-4eac-84ea-a8e1ca36d51b
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA091135
Listing Expiration
2026-12-31
Marketing Start
2012-08-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808384
Hyphenated Format
37808-384
Supplemental Identifiers
RxCUI
UNII
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
cough dm (source: ndc)
Generic Name
dextromethorphan polistirex (source: ndc)
Application Number
ANDA091135 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/5mL
Packaging
- 1 BOTTLE in 1 CARTON (37808-384-21) / 89 mL in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (37808-384-28) / 148 mL in 1 BOTTLE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "76f9d0f8-2bb8-4eac-84ea-a8e1ca36d51b", "openfda": {"unii": ["9D2RTI9KYH"], "rxcui": ["1373045"], "spl_set_id": ["f8f225cd-a0f2-4991-828f-cc7549778235"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-384-21) / 89 mL in 1 BOTTLE", "package_ndc": "37808-384-21", "marketing_start_date": "20120830"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-384-28) / 148 mL in 1 BOTTLE", "package_ndc": "37808-384-28", "marketing_start_date": "20160413"}], "brand_name": "Cough DM", "product_id": "37808-384_76f9d0f8-2bb8-4eac-84ea-a8e1ca36d51b", "dosage_form": "SUSPENSION", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "37808-384", "generic_name": "dextromethorphan polistirex", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cough DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/5mL"}], "application_number": "ANDA091135", "marketing_category": "ANDA", "marketing_start_date": "20120830", "listing_expiration_date": "20261231"}