NDC 70710-2139-01 - Carbidopa and Levodopa

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
70710-2139
Requested NDC
70710-2139-01
Package NDCs from labels
70710-2139-1, 70710-2139-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-04-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Carbidopa and Levodopa - REMEDYREPACK INC.REMEDYREPACK INC.2026-04-24HUMAN PRESCRIPTION DRUG LABEL
CARBIDOPA - Zydus Pharmaceuticals USA Inc. | Amneal Pharmaceuticals Pvt. Ltd. | Bora Pharmaceutical Laboratories IncZydus Pharmaceuticals USA Inc. | Amneal Pharmaceuticals Pvt. Ltd. | Bora Pharmaceutical Laboratories Inc2025-11-14HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70710-2139-1Carbidopa and Levodopa100 in 1 BOTTLECAPSULE, EXTENDED RELEASE1002

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70710-2139-1EA - Each70710-2139374b83f9-e6ba-45b3-ac20-0925ca6a50ee12025-11-13

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 279 of 279 · 5,563 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Renewal Firming Day Broad Spectrum SPF 30TITANIUM DIOXIDE, ZINC OXIDEBURT'S BEES, INC.18ceb5d8-4b76-6a54-e054-00144ff88e882015-06-18WarningsExact identifier
unii: 15FIX9V2JP
Instant Hand SanitizerALCOHOLSafetec of America, Inc.f9e30645-491b-4f54-acfd-f863ee2356072013-08-07WarningsExact identifier
unii: 3K9958V90M
TiZO2TITANIUM DIOXIDE, ZINC OXIDEFallien Cosmeceuticals, LTD.30468afc-9616-4765-b046-12e97a0a78272010-12-20WarningsExact identifier
unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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