misoprostol
Generic: misoprostol
Labeler: redpharm drugDrug Facts
Product Profile
Brand Name
misoprostol
Generic Name
misoprostol
Labeler
redpharm drug
Dosage Form
TABLET
Routes
Active Ingredients
misoprostol 200 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
67296-1936
Product ID
67296-1936_46e93923-334c-68db-e063-6394a90ad902
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA019268
Listing Expiration
2026-12-31
Marketing Start
2009-12-27
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
672961936
Hyphenated Format
67296-1936
Supplemental Identifiers
RxCUI
UNII
NUI
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
NDA019268 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 ug/1
Packaging
- 10 TABLET in 1 BOTTLE (67296-1936-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46e93923-334c-68db-e063-6394a90ad902", "openfda": {"nui": ["N0000175785", "M0017811"], "unii": ["0E43V0BB57"], "rxcui": ["317128"], "spl_set_id": ["2fd197c6-05db-5011-e063-6294a90a585d"], "pharm_class_cs": ["Prostaglandins E, Synthetic [CS]"], "pharm_class_epc": ["Prostaglandin E1 Analog [EPC]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (67296-1936-1)", "package_ndc": "67296-1936-1", "marketing_start_date": "20091227"}], "brand_name": "misoprostol", "product_id": "67296-1936_46e93923-334c-68db-e063-6394a90ad902", "dosage_form": "TABLET", "pharm_class": ["Prostaglandin E1 Analog [EPC]", "Prostaglandins E", "Synthetic [CS]"], "product_ndc": "67296-1936", "generic_name": "MISOPROSTOL", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "misoprostol", "active_ingredients": [{"name": "MISOPROSTOL", "strength": "200 ug/1"}], "application_number": "NDA019268", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20091227", "listing_expiration_date": "20261231"}