NDC 67787-272 - Ramipril

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
67787-272
Package NDCs from labels
67787-272-01, 67787-272-10
Manufacturer
InvaGen Pharmaceuticals, Inc
Effective date
2008-07-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ramipril - InvaGen Pharmaceuticals, IncInvaGen Pharmaceuticals, Inc2008-07-23HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67787-272-01Ramipril100 in 1 BOTTLECAPSULE1001
67787-272-10Ramipril1000 in 1 BOTTLECAPSULE10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67787-272RAMIPRIL (RAMIPRIL) CAPSULE [INVAGEN PHARMACEUTICALS, INC]12 package rows20080904_8b59207a-ea5c-4697-a8b6-94c3015a00de.zip

DailyMed Socrata Ingredients#

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 2 of 2 · 35 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RamiprilRAMIPRILNorthwind Health Company, LLCab324cb3-2aaa-b57f-e053-2995a90a20552026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198188
RamiprilRAMIPRILNorthwind Health Company, LLCfb0892da-3db7-3202-e053-6394a90ab6052026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 261962
RamiprilRAMIPRILA-S Medication Solutions5fb23b7d-ed2b-4984-89c8-d0a509b917e12025-12-23Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198188
RamiprilRAMIPRILGSMS, Incorporated62f6aa5a-7587-4349-b61d-b2c2357499792025-07-10Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198188
rxcui: 198189
rxcui: 261962
RamiprilRAMIPRILA-S Medication Solutions1576188e-efd4-4e14-870e-fd9bd2751c452025-04-14Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198189
rxcui: 261962
RamiprilRAMIPRILA-S Medication Solutionsdd3162eb-5f09-47ac-9efd-3ddeee695a252025-04-14Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 261962
RamiprilRAMIPRILZydus Lifesciences Limited496b346b-ca79-4483-a950-bed9464e6a9d2024-12-04Exact identifier
rxcui: 198188
rxcui: 198189
rxcui: 845488
rxcui: 261962
RamiprilRAMIPRILA-S Medication Solutions4a91b706-c614-4472-92f2-4da5d7bdbf272024-11-21Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198188
RamiprilRAMIPRILProficient Rx LP01da05d8-e72e-4208-bf92-a5cd929f15ab2022-07-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198189
rxcui: 261962
RamiprilRAMIPRILExelan Pharmaceuticals, Inc.1e1dfacf-b831-4743-a874-9a5e5ef8a1202021-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198188
rxcui: 198189
rxcui: 845488
rxcui: 261962
RamiprilRAMIPRILProficient Rx LP33bdfe96-1b7a-4859-b1c9-ef94b8bb7a2a2019-11-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198188
RamiprilRAMIPRILProficient Rx LPafd766bc-2a42-40b5-b33f-1a8b5ce2622e2019-11-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 261962
RamiprilRAMIPRILProficient Rx LP543914e5-c164-4fc7-8007-9fab2b13dda72019-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 261962
RamiprilRAMIPRILProficient Rx LPd3513b8b-2d8a-456d-b942-a25ec1965b042019-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198188
32CAE3AE-8AF3-54C0-E4D2-70CBE21748738b59207a-ea5c-4697-a8b6-94c3015a00de2008-07-23Boxed warning, Warnings, Adverse reactionsExact identifier
spl id: 32CAE3AE-8AF3-54C0-E4D2-70CBE2174873
spl set id: 8b59207a-ea5c-4697-a8b6-94c3015a00de

Reported adverse events (FAERS/openFDA)#

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