misoprostol
Generic: misoprostol
Labeler: avpakDrug Facts
Product Profile
Brand Name
misoprostol
Generic Name
misoprostol
Labeler
avpak
Dosage Form
TABLET
Routes
Active Ingredients
misoprostol 200 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
50268-555
Product ID
50268-555_47e7448c-f84c-4a4c-e063-6394a90ad262
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210201
Listing Expiration
2027-12-31
Marketing Start
2024-10-03
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50268555
Hyphenated Format
50268-555
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
misoprostol (source: ndc)
Generic Name
misoprostol (source: ndc)
Application Number
ANDA210201 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 ug/1
Packaging
- 60 TABLET in 1 BOTTLE (50268-555-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e7448c-f84c-4a4c-e063-6394a90ad262", "openfda": {"nui": ["N0000175785", "M0017811"], "upc": ["0350268555607"], "unii": ["0E43V0BB57"], "rxcui": ["317128"], "spl_set_id": ["2396e9c0-3742-69cf-e063-6394a90adb13"], "pharm_class_cs": ["Prostaglandins E, Synthetic [CS]"], "pharm_class_epc": ["Prostaglandin E1 Analog [EPC]"], "manufacturer_name": ["AvPAK"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50268-555-60)", "package_ndc": "50268-555-60", "marketing_start_date": "20241003"}], "brand_name": "Misoprostol", "product_id": "50268-555_47e7448c-f84c-4a4c-e063-6394a90ad262", "dosage_form": "TABLET", "pharm_class": ["Prostaglandin E1 Analog [EPC]", "Prostaglandins E", "Synthetic [CS]"], "product_ndc": "50268-555", "generic_name": "Misoprostol", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Misoprostol", "active_ingredients": [{"name": "MISOPROSTOL", "strength": "200 ug/1"}], "application_number": "ANDA210201", "marketing_category": "ANDA", "marketing_start_date": "20241003", "listing_expiration_date": "20271231"}