FDA.reportPublic FDA data

NDC 69339-160-01 - Megestrol Acetate

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
69339-160
Requested NDC
69339-160-01
Package NDCs from labels
69339-160-01, 69339-160-16, 69339-160-17, 69339-160-18, 69339-160-19
Manufacturer
Natco Pharma USA LLC | Strides Pharma, Inc
Effective date
2026-01-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Megestrol Acetate - Natco Pharma USA LLC | Strides Pharma, IncNatco Pharma USA LLC | Strides Pharma, Inc2026-01-15HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDCRelated label
69339-160-16MEGESTROL ACETATE ORAL SUSPENSION, USP
69339-160-17MEGESTROL ACETATE ORAL SUSPENSION, USP
69339-160-18MEGESTROL ACETATE ORAL SUSPENSION, USP
69339-160-19MEGESTROL ACETATE ORAL SUSPENSION, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69339-160-01Megestrol Acetate10 mL in 1 CUP, UNIT-DOSESUSPENSION102
69339-160-16Megestrol Acetate3 in 1 CASESUSPENSION32
69339-160-16Megestrol Acetate10 in 1 TRAYSUSPENSION102
69339-160-17Megestrol Acetate4 in 1 CASESUSPENSION42
69339-160-17Megestrol Acetate10 in 1 TRAYSUSPENSION102
69339-160-18Megestrol Acetate10 in 1 TRAYSUSPENSION102
69339-160-18Megestrol Acetate5 in 1 CASESUSPENSION52
69339-160-19Megestrol Acetate10 in 1 CASESUSPENSION102
69339-160-19Megestrol Acetate10 in 1 TRAYSUSPENSION102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69339-160MEGESTROL ACETATE SUSPENSION [NATCO PHARMA USA LLC]1Current NDC, 9 package rows20230825_582cff8a-1def-43d6-ba7e-dce49e3e9f27.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69339-160-01ML - Milliliter69339-16067edb6da-5e2c-4fcc-8a4a-3b098aaff6eb12023-09-05
69339-160-16ML - Milliliter69339-16027f6e6c7-08d3-442e-b959-3a663f18545312023-09-05
69339-160-17ML - Milliliter69339-16031b3dcc7-2913-4c24-b3a6-640158ec6c3712023-09-05
69339-160-18ML - Milliliter69339-16059fcc138-63c5-45d5-b946-93f453f5505612023-09-05
69339-160-19ML - Milliliter69339-160da7e552a-6eec-4c7f-993b-b3d609d66d9912023-09-05

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 29 of 39 · 767 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Docusate SodiumDOCUSATE SODIUMNuCare Pharmaceuticals,Inc.56f7966a-c95e-3ce3-e054-00144ff88e882024-08-14WarningsExact identifier
unii: F05Q2T2JA0
Sool Softener LaxativeDOCUSATE SODIUM, SENNOSIDESEQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)7104b955-fadd-4ce7-9342-fb28027fc4a92024-08-12WarningsExact identifier
unii: F05Q2T2JA0
Senna S OrangeDOCUSATE SODIUM SENNOSIDESCare One (Retail Business Services, LLC.)3da76cb2-08c3-475d-9320-69450bbcf8cd2024-08-09WarningsExact identifier
unii: F05Q2T2JA0
Senna PlusDOCUSATE SODIUM, SENNOSIDESAmerisourceBergen (Good Neighbor Pharmacy) 4612268bf0d90-db4b-48f0-bce1-80127922bc822024-08-09WarningsExact identifier
unii: F05Q2T2JA0
Senna SDOCUSATE SODIUM, SENNOSIDESUnited Natural Foods, Inc. dba UNFI3f519d42-72bc-4cc3-a43f-14b94a10eb9a2024-08-09WarningsExact identifier
unii: F05Q2T2JA0
Stool Softener plus LaxativeDOCUSATE SODIUM, SENNOSIDESQUALITY CHOICE (Chain Drug Marketing Association)ebb35e67-4e83-445e-af6e-ecb43b1d3df62024-08-09WarningsExact identifier
unii: F05Q2T2JA0
Senna SDOCUSATE SODIUM, SENNOSIDESTOP CARE (Topco Associates LLC)3984f4aa-2794-410c-ae9e-ee5bc31c04702024-08-09WarningsExact identifier
unii: F05Q2T2JA0
Up and Up Hemorrhoid MAX STRENGTH14.4% GLYCERIN, 0.25% PHENYLEPHRINE HCL, 1% PRAMOXINE HCL, 15% PETROLATUMTarget Corporation867677b5-fd1d-449e-966e-1de0b5c98afb2024-08-08WarningsExact identifier
unii: PDC6A3C0OX
Stool Softener LaxativeDOCUSATE SODIUM AND SENNOSIDESWinCo Foods, LLC2776d463-753d-4fee-ab5e-210ce36044112024-08-07WarningsExact identifier
unii: F05Q2T2JA0
Stool Softener with laxativeDOCUSATE SODIUM AND SENNOSIDESWinCo Foods, LLC3803830c-187d-4403-9606-db036418386f2024-08-07WarningsExact identifier
unii: F05Q2T2JA0
Stool Softener LaxativeDOCUSATE SODIUMProficient Rx LPccfa095c-77f0-41ff-84f8-e02d983c7c742024-08-01WarningsExact identifier
unii: F05Q2T2JA0
Stool SoftenerDOCUSATE SODIUM SENNOSIDESQUALITY CHOICE (Chain Drug Marketing Association)d4128fbd-32ba-4d2e-ae1a-cbe438f5b39b2024-07-31WarningsExact identifier
unii: F05Q2T2JA0
Stool Softener Laxative Plus StimulantDOCUSATE SODIUM AND SENNOSIDESWalgreensdb528659-768a-46e0-a340-9fbcdb25ea5e2024-07-25WarningsExact identifier
unii: F05Q2T2JA0
Stimulant Laxative Plus Stool SoftenerDOCUSATE SODIUM AND SENNOSIDESGOOD SENSE17cdef7b-71bf-b4a6-e063-6294a90a5b742024-07-22WarningsExact identifier
unii: F05Q2T2JA0
Sodium Citrate and Citric AcidSODIUM CITRATE AND CITRIC ACID MONOHYDRATEAmerican Health Packaging58fa9952-c8ab-4ebb-a073-15cc45f4832a2024-07-16Adverse reactionsExact identifier
unii: 1Q73Q2JULR
Stool SoftenerDOCUSATE SODIUM AND SENNOSIDESStrategic Sourcing Services LLCb23e53d4-fd7d-452d-a851-35a143b6dcb42024-07-08WarningsExact identifier
unii: F05Q2T2JA0
Zenibell Snail IntensiveCreamGLYCERINMISOCOS97c19dca-237c-c968-e053-2a95a90aeae72024-07-05WarningsExact identifier
unii: PDC6A3C0OX
Zenibell Snail Intensive TonerGLYCERINMISOCOS97c1b556-824d-bef7-e053-2a95a90ae1f22024-07-05WarningsExact identifier
unii: PDC6A3C0OX
aewajin Derma HydrocellGLYCERINMISOCOS980fcaea-27ba-da49-e053-2995a90ad5062024-07-05WarningsExact identifier
unii: PDC6A3C0OX
aewajin Derma Hydrocell 24k Gold SerumGLYCERINMISOCOSa17b2c6e-9db8-bae4-e053-2a95a90adcf62024-07-05WarningsExact identifier
unii: PDC6A3C0OX

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.