ibuprofen
Generic: ibuprofen
Labeler: granules india limitedDrug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
granules india limited
Dosage Form
TABLET
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62207-321
Product ID
62207-321_44a726e4-0a4b-b303-e063-6394a90a9073
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA202312
Listing Expiration
2026-12-31
Marketing Start
2019-11-14
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62207321
Hyphenated Format
62207-321
Supplemental Identifiers
RxCUI
UPC
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 (source: ndc)
Generic Name
ibuprofen (source: ndc)
Application Number
ANDA202312 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 24 TABLET in 1 BOTTLE (62207-321-41)
- 50 TABLET in 1 BOTTLE (62207-321-42)
- 100 TABLET in 1 BOTTLE (62207-321-43)
- 250 TABLET in 1 BOTTLE (62207-321-46)
- 500 TABLET in 1 BOTTLE (62207-321-47)
- 750 TABLET in 1 BOTTLE (62207-321-48)
- 1000 TABLET in 1 BOTTLE (62207-321-49)
- 10 TABLET in 1 BOTTLE (62207-321-89)
- 1700 TABLET in 1 BOTTLE (62207-321-90)
- 160000 TABLET in 1 DRUM (62207-321-91)
Packages (10)
62207-321-41
24 TABLET in 1 BOTTLE (62207-321-41)
62207-321-42
50 TABLET in 1 BOTTLE (62207-321-42)
62207-321-43
100 TABLET in 1 BOTTLE (62207-321-43)
62207-321-46
250 TABLET in 1 BOTTLE (62207-321-46)
62207-321-47
500 TABLET in 1 BOTTLE (62207-321-47)
62207-321-48
750 TABLET in 1 BOTTLE (62207-321-48)
62207-321-49
1000 TABLET in 1 BOTTLE (62207-321-49)
62207-321-89
10 TABLET in 1 BOTTLE (62207-321-89)
62207-321-90
1700 TABLET in 1 BOTTLE (62207-321-90)
62207-321-91
160000 TABLET in 1 DRUM (62207-321-91)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44a726e4-0a4b-b303-e063-6394a90a9073", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0362207321464", "0362207320467"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["97516b9f-219a-429d-850d-1fe9fd66646b"], "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": ["Granules India Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET in 1 BOTTLE (62207-321-41)", "package_ndc": "62207-321-41", "marketing_start_date": "20191114"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (62207-321-42)", "package_ndc": "62207-321-42", "marketing_start_date": "20191114"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62207-321-43)", "package_ndc": "62207-321-43", "marketing_start_date": "20191114"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE (62207-321-46)", "package_ndc": "62207-321-46", "marketing_start_date": "20191114"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (62207-321-47)", "package_ndc": "62207-321-47", "marketing_start_date": "20191114"}, {"sample": false, "description": "750 TABLET in 1 BOTTLE (62207-321-48)", "package_ndc": "62207-321-48", "marketing_start_date": "20191114"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62207-321-49)", "package_ndc": "62207-321-49", "marketing_start_date": "20191114"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (62207-321-89)", "package_ndc": "62207-321-89", "marketing_start_date": "20201203"}, {"sample": false, "description": "1700 TABLET in 1 BOTTLE (62207-321-90)", "package_ndc": "62207-321-90", "marketing_start_date": "20201203"}, {"sample": false, "description": "160000 TABLET in 1 DRUM (62207-321-91)", "package_ndc": "62207-321-91", "marketing_start_date": "20191114"}], "brand_name": "IBUPROFEN", "product_id": "62207-321_44a726e4-0a4b-b303-e063-6394a90a9073", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "62207-321", "generic_name": "IBUPROFEN", "labeler_name": "Granules India Limited", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA202312", "marketing_category": "ANDA", "marketing_start_date": "20191114", "listing_expiration_date": "20261231"}