ibuprofen, diphenhydramine hcl
Generic: ibuprofen, diphenhydramine hcl
Labeler: rite aid corporationDrug Facts
Product Profile
Brand Name
ibuprofen, diphenhydramine hcl
Generic Name
ibuprofen, diphenhydramine hcl
Labeler
rite aid corporation
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
diphenhydramine hydrochloride 25 mg/1, ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
11822-0789
Product ID
11822-0789_a35f6b2b-8e67-dd2d-e053-2995a90a27e1
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA090397
Listing Expiration
2026-12-31
Marketing Start
2020-04-15
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
118220789
Hyphenated Format
11822-0789
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
ibuprofen, diphenhydramine hcl (source: ndc)
Generic Name
ibuprofen, diphenhydramine hcl (source: ndc)
Application Number
ANDA090397 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
- 200 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (11822-0789-4) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a35f6b2b-8e67-dd2d-e053-2995a90a27e1", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["TC2D6JAD40", "WK2XYI10QM"], "rxcui": ["901814"], "spl_set_id": ["a35f68f3-c7f8-a55f-e053-2a95a90a9047"], "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": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-0789-4) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "11822-0789-4", "marketing_start_date": "20200415"}], "brand_name": "IBUPROFEN, DIPHENHYDRAMINE HCL", "product_id": "11822-0789_a35f6b2b-8e67-dd2d-e053-2995a90a27e1", "dosage_form": "CAPSULE, LIQUID FILLED", "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": "11822-0789", "generic_name": "IBUPROFEN, DIPHENHYDRAMINE HCL", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN, DIPHENHYDRAMINE HCL", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA090397", "marketing_category": "ANDA", "marketing_start_date": "20200415", "listing_expiration_date": "20261231"}