Home NDC 70518-1377 Carvedilol
Product NDC 70518-1377
11-digit product format 705181377
Labeler code 70518
Product ID 70518-1377_55f1f987-ff0f-be6e-e063-6294a90afebe
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Carvedilol
Dosage form TABLET, FILM COATED
Route ORAL
Labeler REMEDYREPACK INC.
Application ANDA077614
Marketing category ANDA
Marketing start 2018-08-15
Substance CARVEDILOL
Active strength 3.125 mg/1
Pharmacologic classes Adrenergic alpha-Antagonists [MoA], Adrenergic beta1-Antagonists [MoA], Adrenergic beta2-Antagonists [MoA], alpha-Adrenergic Blocker [EPC], beta-Adrenergic Blocker [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes
Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 23 matching rows.
View current auxiliary records. · View the auxiliary file history.
Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 4 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A077614-001 CARVEDILOL CARVEDILOL 6.25MG TABLET / ORAL AB 2007-09-05 A077614-002 CARVEDILOL CARVEDILOL 12.5MG TABLET / ORAL AB 2007-09-05 A077614-003 CARVEDILOL CARVEDILOL 25MG TABLET / ORAL AB 2007-09-05 A077614-004 CARVEDILOL CARVEDILOL 3.125MG TABLET / ORAL AB 2007-09-05
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 4 matching rows.
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 1 of 5 · 172 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-09-14 22:38:34 2026-08 A077614-001 CARVEDILOL 6.25MG TABLET / ORAL AB 2007-09-05 84e616aacf4f…2026-09-14 22:38:34 2026-08 A077614-002 CARVEDILOL 12.5MG TABLET / ORAL AB 2007-09-05 84e616aacf4f…2026-09-14 22:38:34 2026-08 A077614-003 CARVEDILOL 25MG TABLET / ORAL AB 2007-09-05 84e616aacf4f…2026-09-14 22:38:34 2026-08 A077614-004 CARVEDILOL 3.125MG TABLET / ORAL AB 2007-09-05 84e616aacf4f…2026-08-18 06:07:40 2026-07 A077614-001 CARVEDILOL 6.25MG TABLET / ORAL AB 2007-09-05 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A077614-002 CARVEDILOL 12.5MG TABLET / ORAL AB 2007-09-05 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A077614-003 CARVEDILOL 25MG TABLET / ORAL AB 2007-09-05 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A077614-004 CARVEDILOL 3.125MG TABLET / ORAL AB 2007-09-05 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A077614-001 CARVEDILOL 6.25MG TABLET / ORAL AB 2007-09-05 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A077614-002 CARVEDILOL 12.5MG TABLET / ORAL AB 2007-09-05 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A077614-003 CARVEDILOL 25MG TABLET / ORAL AB 2007-09-05 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A077614-004 CARVEDILOL 3.125MG TABLET / ORAL AB 2007-09-05 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077614-001 CARVEDILOL 6.25MG TABLET / ORAL AB 2007-09-05 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077614-002 CARVEDILOL 12.5MG TABLET / ORAL AB 2007-09-05 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077614-003 CARVEDILOL 25MG TABLET / ORAL AB 2007-09-05 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077614-004 CARVEDILOL 3.125MG TABLET / ORAL AB 2007-09-05 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A077614-001 CARVEDILOL 6.25MG TABLET / ORAL AB 2007-09-05 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A077614-002 CARVEDILOL 12.5MG TABLET / ORAL AB 2007-09-05 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A077614-003 CARVEDILOL 25MG TABLET / ORAL AB 2007-09-05 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A077614-004 CARVEDILOL 3.125MG TABLET / ORAL AB 2007-09-05 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077614-001 CARVEDILOL 6.25MG TABLET / ORAL AB 2007-09-05 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077614-002 CARVEDILOL 12.5MG TABLET / ORAL AB 2007-09-05 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077614-003 CARVEDILOL 25MG TABLET / ORAL AB 2007-09-05 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077614-004 CARVEDILOL 3.125MG TABLET / ORAL AB 2007-09-05 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077614-001 CARVEDILOL 6.25MG TABLET / ORAL AB 2007-09-05 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077614-002 CARVEDILOL 12.5MG TABLET / ORAL AB 2007-09-05 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077614-003 CARVEDILOL 25MG TABLET / ORAL AB 2007-09-05 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077614-004 CARVEDILOL 3.125MG TABLET / ORAL AB 2007-09-05 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077614-001 CARVEDILOL 6.25MG TABLET / ORAL AB 2007-09-05 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077614-002 CARVEDILOL 12.5MG TABLET / ORAL AB 2007-09-05 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077614-003 CARVEDILOL 25MG TABLET / ORAL AB 2007-09-05 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077614-004 CARVEDILOL 3.125MG TABLET / ORAL AB 2007-09-05 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077614-001 CARVEDILOL 6.25MG TABLET / ORAL AB 2007-09-05 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077614-002 CARVEDILOL 12.5MG TABLET / ORAL AB 2007-09-05 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077614-003 CARVEDILOL 25MG TABLET / ORAL AB 2007-09-05 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077614-004 CARVEDILOL 3.125MG TABLET / ORAL AB 2007-09-05 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077614-001 CARVEDILOL 6.25MG TABLET / ORAL AB 2007-09-05 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077614-002 CARVEDILOL 12.5MG TABLET / ORAL AB 2007-09-05 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077614-003 CARVEDILOL 25MG TABLET / ORAL AB 2007-09-05 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077614-004 CARVEDILOL 3.125MG TABLET / ORAL AB 2007-09-05 5bbf6a4d5a75…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 5 · 172 observed states.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Carvedilol
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CARVEDILOL 3.125 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0K47UL67F2 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 686924 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70518-1377-0 Carvedilol 30 in 1 BLISTER PACK TABLET, FILM COATED 30 19 70518-1377-1 Carvedilol 180 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 180 19 70518-1377-2 Carvedilol 90 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 90 19 70518-1377-3 Carvedilol 100 in 1 BOX TABLET, FILM COATED 100 19 70518-1377-4 Carvedilol 1 in 1 POUCH TABLET, FILM COATED 1 19 70518-1377-5 Carvedilol 100 in 1 BOX TABLET, FILM COATED 100 19 70518-1377-6 Carvedilol 1 in 1 POUCH TABLET, FILM COATED 1 19 70518-1377-7 Carvedilol 50 in 1 BOX TABLET, FILM COATED 50 19
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70518-1377 CARVEDILOL TABLET, FILM COATED [REMEDYREPACK INC.] 17 Current NDC, Legacy NDC, 8 package rows 20250524_32098c09-7580-4975-a3e1-31b619c04c69.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 3 of 3 · 45 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Carvedilol CARVEDILOL Bryant Ranch Prepack da830b08-1cdd-4d36-a068-c376fd7763c4 2024-08-22 Warnings, Adverse reactions Exact identifier application applno (ANDA): 077614 application number: ANDA077614 Carvedilol CARVEDILOL Proficient Rx LP 0bfea06d-7abe-407a-80a4-d15d373569f7 2024-07-01 Warnings, Adverse reactions Exact identifier application applno (ANDA): 077614 application number: ANDA077614 Carvedilol CARVEDILOL NuCare Pharmaceuticals,Inc. e31271aa-259b-caa6-e053-2995a90a0fcd 2024-06-28 Warnings, Adverse reactions Exact identifier application applno (ANDA): 077614 application number: ANDA077614 Carvedilol CARVEDILOL NuCare Pharmaceuticals,Inc. 8ccf07f5-78fb-76da-e053-2a95a90a0090 2024-06-18 Warnings, Adverse reactions Exact identifier application applno (ANDA): 077614 application number: ANDA077614 Carvedilol CARVEDILOL NuCare Pharmaceuticals, Inc. 49afdf89-0bed-71da-e054-00144ff88e88 2024-01-12 Warnings, Adverse reactions Exact identifier application applno (ANDA): 077614 application number: ANDA077614
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70518-1377-0 70518137700 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1377-0) 2018-08-15 0000-00-00 No No Current 70518-1377-1 70518137701 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1377-1) 2019-07-09 0000-00-00 No No Current 70518-1377-2 70518137702 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1377-2) 2020-01-30 0000-00-00 No No Current 70518-1377-3 70518137703 100 POUCH in 1 BOX (70518-1377-3) > 1 TABLET, FILM COATED in 1 POUCH (70518-1377-4) 100 pouch 2021-08-03 0000-00-00 No No Current 70518-1377-4 70518137704 1 in 1 POUCH Historical 70518-1377-5 70518137705 100 POUCH in 1 BOX (70518-1377-5) / 1 TABLET, FILM COATED in 1 POUCH (70518-1377-6) 100 pouch 2025-05-14 No No Current 70518-1377-6 70518137706 1 in 1 POUCH Historical 70518-1377-7 70518137707 50 POUCH in 1 BOX (70518-1377-7) / 1 TABLET, FILM COATED in 1 POUCH (70518-1377-6) 50 pouch 2026-04-24 No No Current