FDA.reportPublic FDA data

NDC 70710-1233-01 - Betamethasone dipropionate

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
70710-1233
Requested NDC
70710-1233-01
Package NDCs from labels
70710-1233-1, 70710-1233-4, 70710-1233-01
Manufacturer
REMEDYREPACK INC.
Effective date
2025-07-25
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Betamethasone dipropionate - REMEDYREPACK INC.REMEDYREPACK INC.2025-07-25HUMAN PRESCRIPTION DRUG LABEL
Betamethasone dipropionate - A-S Medication SolutionsA-S Medication Solutions2023-12-15HUMAN PRESCRIPTION DRUG LABEL
Betamethasone dipropionate - A-S Medication SolutionsA-S Medication Solutions2023-10-31HUMAN PRESCRIPTION DRUG LABEL
BETAMETHASONE - Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences LimitedZydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited2022-10-05HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70710-1233-1Betamethasone dipropionate15 g in 1 TUBECREAM153
70710-1233-1Betamethasone dipropionate1 in 1 CARTONCREAM13
70710-1233-4Betamethasone dipropionate1 in 1 CARTONCREAM13
70710-1233-4Betamethasone dipropionate45 g in 1 TUBECREAM453

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70710-1233BETAMETHASONE DIPROPIONATE CREAM [ZYDUS PHARMACEUTICALS USA INC.]3Current NDC, Legacy NDC, 4 package rows20221007_18d80661-72ad-4a83-917f-a80ce37a5568.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70710-1233-1GM - Gram70710-123376e92d62-4588-4356-b5ae-513a2a3f263512019-05-02
70710-1233-4GM - Gram70710-1233ae208291-c0e1-424c-a37c-ce2ac84eac8612019-05-02

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 41 of 43 · 847 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Betamethasone dipropionateBETAMETHASONE DIPROPIONATEZydus Pharmaceuticals USA Inc.18d80661-72ad-4a83-917f-a80ce37a55682022-10-05Adverse reactionsExact identifier
application number: ANDA208885
ndc (package): 70710-1233-1
ndc (package): 70710-1233-4
ndc (product): 70710-1233
ndc11 (package): 70710123301
rxcui: 238920
spl id: fecfe1c4-1732-48a4-beaa-6bdc5577731a
spl set id: 18d80661-72ad-4a83-917f-a80ce37a5568
unii: 826Y60901U
Bach Original Flower Remedies Rock WaterWATERNelson Bach USA Limitedea242559-1618-3354-e053-2a95a90a1a952022-10-03WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERMedical Purchasing Solutions, LLCe90b47e3-9636-b9ee-e053-2a95a90ad48c2022-09-19Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
BHI SkinBERBERIS VULGARIS ROOT BARK, GRAPHITE, HYDROFLUORIC ACID, LYCOPODIUM CLAVATUM SPORE, PETROLATUM, TOXICODENDRON PUBESCENS LEAF, SEPIA OFFICINALIS JUICE, AND SULFURMediNatura Inc70ab2931-bd2d-43de-bb36-d019f78e3d732022-07-07WarningsExact identifier
unii: 4T6H12BN9U
REFRESH P.M.MINERAL OIL, PETROLATUMAllergan, Inc.24365d64-cd94-41cc-a7e1-033102d981142022-06-30WarningsExact identifier
unii: 4T6H12BN9U
unii: T5L8T28FGP
Sterile WaterWATERFresenius Kabi USA, LLCf42ac50f-0ec5-4713-a4c8-99d972d90bed2022-06-22Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERFresenius Kabi USA, LLCe71c6c83-d518-496c-b2ab-efd5987e47832022-06-09Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Clotrimazole and Betamethasone DipropionateCLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATEProficient Rx LP3d235926-6f17-4aa5-be82-7f1b4357e2472022-06-01Adverse reactionsExact identifier
unii: 826Y60901U
Betamethasone DipropionateBETAMETHASONE DIPROPIONATEProficient Rx LPf1be7c91-5408-4d31-8673-b691089aadce2022-04-01Warnings, Adverse reactionsExact identifier
unii: 826Y60901U
Betamethasone DipropionateBETAMETHASONE DIPROPIONATEPadagis Israel Pharmaceuticals Ltde6018480-7788-472d-a2d1-ccccffcd258e2022-02-28Adverse reactionsExact identifier
unii: 826Y60901U
Sterile WaterWATERAmerican Regent, Inc.78b35864-4bbc-4759-a5c1-7e4f25e229322022-01-31Boxed warningExact identifier
unii: 059QF0KO0R
Sterile Diluent for TreprostinilWATERDr.Reddy's Laboratories Inc.,33050ee2-519b-1f0b-d4df-9e14dd329c572021-12-23Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
ENSTILARCALCIPOTRIENE AND BETAMETHASONE DIPROPIONATELEO Pharma Inc.d1193df2-d53f-4342-bd9d-d9cba7c897092021-10-18Warnings, Adverse reactionsExact identifier
unii: 826Y60901U
Sterile WaterSTERILE WATERB. Braun Medical Inc.d99f9133-e4d0-4dee-b611-dbc3f918b5472021-08-09Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERB. Braun Medical Inc.8924e52e-8622-4ed6-a061-1908183e0a182021-08-06Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
EyewashEYEWASHGlobal Equipment Companyc4f78121-4668-2e0c-e053-2995a90ab6c62021-06-17WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERAsclemed USA, Inc.45c38269-883c-4198-a9d5-03810a4420ec2021-01-14Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Clotrimazole and Betamethasone DipropionateCLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATEProficient Rx LPc6e4bf5f-f6d6-489e-9286-c30568c601b72021-01-01Warnings, Adverse reactionsExact identifier
unii: 826Y60901U
Clotrimazole and Betamethasone DipropionateCLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATEGlenmark Pharmaceuticals Inc. USA8dcd24cb-e568-428a-88ac-737d115cc54d2020-11-09Warnings, Adverse reactionsExact identifier
unii: 826Y60901U
Betamethasone DipropionateBETAMETHASONE DIPROPIONATEGlenmark Pharmaceuticals Inc., USA78bdb7ca-acb0-491c-bed9-4ebbf2a079182020-08-31Warnings, Adverse reactionsExact identifier
unii: 826Y60901U

Reported adverse events (FAERS/openFDA)#

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