FDA.reportPublic FDA data

NDC 17856-0060-2 - 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
17856-0060
Requested NDC
17856-0060-2
Package NDCs from labels
17856-0060-1, 17856-0060-3, 17856-0060-2, 17856-0060-4
Manufacturer
ATLANTIC BIOLOGICALS CORP.
Effective date
2026-07-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
MEGESTROL ACETATE ORAL SUSPENSION, USPATLANTIC BIOLOGICALS CORP.2026-07-09HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
17856-0060-32024-05-09MEGESTROL ACETATE ORAL SUSPENSION, USP
17856-0060-32024-05-09MEGESTROL ACETATE ORAL SUSPENSION, USP
17856-0060-42024-05-09MEGESTROL ACETATE ORAL SUSPENSION, USP
17856-0060-42024-05-09MEGESTROL ACETATE ORAL SUSPENSION, USP
17856-0060-32024-01-30MEGESTROL ACETATE ORAL SUSPENSION, USP
17856-0060-32024-01-30MEGESTROL ACETATE ORAL SUSPENSION, USP
17856-0060-42024-01-30MEGESTROL ACETATE ORAL SUSPENSION, USP
17856-0060-42024-01-30MEGESTROL ACETATE ORAL SUSPENSION, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17856-0060-1Megestrol Acetate10 mL in 1 CUPSUSPENSION103
17856-0060-2Megestrol Acetate20 mL in 1 CUPSUSPENSION203
17856-0060-3Megestrol Acetate72 in 1 BOXSUSPENSION723
17856-0060-4Megestrol Acetate50 in 1 BOXSUSPENSION503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17856-0060MEGESTROL ACETATE SUSPENSION [ATLANTIC BIOLOGICALS CORP.]3Current NDC, Legacy NDC, 4 package rows20250524_01119031-9943-4afb-8b45-cb71682f0482.zip

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 35 of 39 · 763 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
OracitCITRIC ACID AND SODIUM CITRATECMP Pharma, Inc.bc26abed-8e6e-475d-8ab3-abf7d03770032023-12-07Adverse reactionsExact identifier
unii: 2968PHW8QP
Stool Softener with LaxativeDOCUSATE SODIUM AND SENNOSIDESGeri-Care Pharmaceutical Corp99fe8064-23f4-5d94-e053-2995a90a66412023-12-06WarningsExact identifier
unii: F05Q2T2JA0
Hemorrhoidal Pain Relief CreamGLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUMWALGREENS03bbe146-f185-bcfa-e063-6394a90a85bf2023-12-04WarningsExact identifier
unii: PDC6A3C0OX
SENNA-SSENNOSIDES AND DOCUSATE SODIUMSTRATEGIC SOURCING SERVICES LLCf9c8e696-c96c-a80f-e053-6394a90a7c922023-11-30WarningsExact identifier
unii: F05Q2T2JA0
Bloop Hemorrhoid Relief TopicalGLYCERIN, PETROLATUM, PHENYLEPHRINE HCL, PRAMOXINE HCLThree Nations Corp0b6419e3-f1c7-bdfe-e063-6294a90a5d922023-11-30WarningsExact identifier
unii: PDC6A3C0OX
SankaijoDOCUSATE SODIUM, SENNOSIDESSato Pharmaceutical Co., Ltd.83c0d52b-f7e2-40b0-a01b-1ccee78f8f1b2023-11-29WarningsExact identifier
unii: F05Q2T2JA0
PhexxiLACTIC ACID, L-, CITRIC ACID MONOHYDRATE, AND POTASSIUM BITARTRATEEvofem, Inc.173ff411-7227-47b0-94dc-844e1ebaf14e2023-11-21Warnings, Adverse reactionsExact identifier
unii: 2968PHW8QP
Stool SoftenerDOCUSATE SODIUMGeri-Care Pharmaceutical Corpb595063a-5fee-18c2-e053-2a95a90a5b992023-11-15WarningsExact identifier
unii: F05Q2T2JA0
Saccharum officinaleSUCROSEBoiron86d04552-b31a-0fcf-e053-2991aa0acecd2023-11-14Exact identifier
unii: C151H8M554
Saccharum officinaleSUCROSEBoiron86d05561-6f09-6f1f-e053-2a91aa0a4b982023-11-14Exact identifier
unii: C151H8M554
DOCUZENSENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MGProficient Rx LP92879e62-f60a-4ab4-9532-610cdd2628ee2023-11-01WarningsExact identifier
unii: F05Q2T2JA0
Docusate SodiumDOCUSATE SODIUMA-S Medication Solutions5999904a-6ac8-4d9e-951c-6e64e8cd93eb2023-11-01WarningsExact identifier
unii: F05Q2T2JA0
Sodium phenylacetate and Sodium benzoateSODIUM PHENYLACETATE AND SODIUM BENZOATEZydus Pharmaceuticals USA Inc.0f17c50f-3761-4470-bf3b-63837a287b8a2023-10-30Warnings, Adverse reactionsExact identifier
unii: OJ245FE5EU
Stool Softener Docusate SodiumDOCUSATE SODIUMMagno-Humphries, Inc.a0e6ab9b-fd31-45fd-93d5-b51d705c180a2023-10-27WarningsExact identifier
unii: F05Q2T2JA0
Stool Softener Docusate SodiumDOCUSATE SODIUMMagno-Humphries, Inc.9d22d642-8aed-d17e-e053-2995a90ae1822023-10-27WarningsExact identifier
unii: F05Q2T2JA0
Senna SDOCUSATE SODIUM, SENNOSIDESMagno-Humphries, Inc.9deaf264-6af0-40ba-e053-2a95a90ada0e2023-10-27WarningsExact identifier
unii: F05Q2T2JA0
Family WellnessGLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, PETROLATUMFRONT PHARMACEUTICAL PLCeb1785f4-5876-443b-b175-9b59d65d1a482023-10-26WarningsExact identifier
unii: PDC6A3C0OX
CVS Health Hemorrhoidal CreamGLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUMFRONT PHARMACEUTICAL PLCcb448d78-553c-4e65-80c5-d4b31d7b36612023-10-26WarningsExact identifier
unii: PDC6A3C0OX
Hemorrhoidal CreamGLYCERIN, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE, WHITE PETROLATUMCardinal Health 110, LLC. dba Leader85a51d5c-679e-1959-e053-2a91aa0a76d52023-10-25WarningsExact identifier
unii: PDC6A3C0OX
Family WellnessGLYCERIN, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE, PETROLATUMZhejiang Jingwei Pharmaceutical Co., Ltd.fde9cd90-d63c-4058-b46e-511fecea36ec2023-10-24WarningsExact identifier
unii: PDC6A3C0OX

Reported adverse events (FAERS/openFDA)#

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