ibuprofen

Generic: ibuprofen

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler h e b
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-709
Product ID 37808-709_7ac57cd0-a501-424f-b789-cf5136848e34
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077349
Listing Expiration 2026-12-31
Marketing Start 2006-07-04

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808709
Hyphenated Format 37808-709

Supplemental Identifiers

RxCUI
310965
UNII
WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

Packaging Origin

Original Packager
true

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 (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA077349 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (37808-709-71) / 50 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (1)

37808-709-71 1 BOTTLE in 1 CARTON (37808-709-71) / 50 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Ibuprofen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7ac57cd0-a501-424f-b789-cf5136848e34", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["21567c0f-abba-4a40-a0b9-5ce49b3d9648"], "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": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-709-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "37808-709-71", "marketing_start_date": "20060821"}], "brand_name": "Ibuprofen", "product_id": "37808-709_7ac57cd0-a501-424f-b789-cf5136848e34", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "37808-709", "generic_name": "Ibuprofen", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA077349", "marketing_category": "ANDA", "marketing_start_date": "20060704", "listing_expiration_date": "20261231"}