good sense ibuprofen pm
Generic: diphenhydramine citrate, ibuprofen
Labeler: l. perrigo companyDrug Facts
Product Profile
Brand Name
good sense ibuprofen pm
Generic Name
diphenhydramine citrate, ibuprofen
Labeler
l. perrigo company
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
diphenhydramine citrate 38 mg/1, ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0113-0050
Product ID
0113-0050_c80d2210-786d-4e91-ada6-f89caf3cf6d0
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA079113
Listing Expiration
2026-12-31
Marketing Start
2009-03-05
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01130050
Hyphenated Format
0113-0050
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
good sense ibuprofen pm (source: ndc)
Generic Name
diphenhydramine citrate, 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 (0113-0050-58) / 40 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (0113-0050-60) / 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": "c80d2210-786d-4e91-ada6-f89caf3cf6d0", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["0488786f-9b6b-4935-bb57-bcb2565447f8"], "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": ["L. Perrigo Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0113-0050-58) / 40 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0113-0050-58", "marketing_start_date": "20090305"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0113-0050-60) / 20 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0113-0050-60", "marketing_start_date": "20100507"}], "brand_name": "good sense ibuprofen pm", "product_id": "0113-0050_c80d2210-786d-4e91-ada6-f89caf3cf6d0", "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": "0113-0050", "generic_name": "diphenhydramine citrate, ibuprofen", "labeler_name": "L. Perrigo Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "good sense 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": "20090305", "listing_expiration_date": "20261231"}