dg health ibuprofen pm
Generic: diphenhydramine citrate and ibuprofen
Labeler: dolgencorp incDrug Facts
Product Profile
Brand Name
dg health ibuprofen pm
Generic Name
diphenhydramine citrate and ibuprofen
Labeler
dolgencorp inc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
diphenhydramine citrate 38 mg/1, ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55910-050
Product ID
55910-050_6eea1216-fa5d-4c82-a575-e382356d409d
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA079113
Listing Expiration
2026-12-31
Marketing Start
2010-01-24
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55910050
Hyphenated Format
55910-050
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
dg health ibuprofen pm (source: ndc)
Generic Name
diphenhydramine citrate and ibuprofen (source: ndc)
Application Number
ANDA079113 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 38 mg/1
- 200 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (55910-050-27) / 80 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (55910-050-60) / 20 TABLET, FILM COATED in 1 BOTTLE
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6eea1216-fa5d-4c82-a575-e382356d409d", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["4bbe40de-0957-4705-893d-fcb4191885c9"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Dolgencorp Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-050-27) / 80 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "55910-050-27", "marketing_start_date": "20200319"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-050-60) / 20 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "55910-050-60", "marketing_start_date": "20100124"}], "brand_name": "dg health Ibuprofen pm", "product_id": "55910-050_6eea1216-fa5d-4c82-a575-e382356d409d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "55910-050", "generic_name": "diphenhydramine citrate and ibuprofen", "labeler_name": "Dolgencorp Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "dg health Ibuprofen pm", "active_ingredients": [{"name": "DIPHENHYDRAMINE CITRATE", "strength": "38 mg/1"}, {"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079113", "marketing_category": "ANDA", "marketing_start_date": "20100124", "listing_expiration_date": "20261231"}