Home NDC 63629-2611 Albuterol
Product NDC 63629-2611
11-digit product format 636292611
Labeler code 63629
Product ID 63629-2611_3352d236-01ed-a102-e063-6294a90a2a8d
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name albuterol
Dosage form TABLET
Route ORAL
Labeler Bryant Ranch Prepack
Application ANDA207046
Marketing category ANDA
Marketing start 2018-06-29
Substance ALBUTEROL SULFATE
Active strength 4 mg/1
Pharmacologic classes Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 2 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A207046-001 ALBUTEROL SULFATE ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 A207046-002 ALBUTEROL SULFATE ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 2 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 3 · 82 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 2026-02-19 14:30 UTC 2026-02 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 1e350fbaab3a…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 8072bd15b7f6…2024-05-31 18:47 UTC 2024-05 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 5c6f7cd8ea54…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 5d02ea3f76ae…2022-04-08 23:34 UTC 2022-04 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 4b0b4de00fa7…2022-04-04 05:41 UTC 2022-04 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 74a2ff9319b5…2019-12-13 00:20 UTC 2019-12 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 bb7c543d1eb4…2022-03-09 01:35 UTC 2022-03 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 bb7c543d1eb4…2021-12-28 21:50 UTC 2021-12 A207046-001 ALBUTEROL SULFATE EQ 2MG BASE TABLET / ORAL AB 2018-06-29 782e0a99824c…2021-12-28 21:50 UTC 2021-12 A207046-002 ALBUTEROL SULFATE EQ 4MG BASE TABLET / ORAL AB 2018-06-29 782e0a99824c…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 3 · 82 observed states.
Additional Listing Data#
Finished product Yes
Brand name base Albuterol
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALBUTEROL SULFATE 4 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 021SEF3731 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 197318 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 63629-2611-1 Albuterol 20 in 1 BOTTLE TABLET 20 102 63629-2611-2 Albuterol 30 in 1 BOTTLE TABLET 30 102 63629-2611-3 Albuterol 60 in 1 BOTTLE TABLET 60 102
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63629-2611 ALBUTEROL TABLET [BRYANT RANCH PREPACK] 102 Current NDC, Legacy NDC, 3 package rows 20250423_601a18ed-d66e-498f-a804-f1a3330827d4.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 1 of 1 · 3 matching rows.
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 63629-2611-1 63629261101 20 TABLET in 1 BOTTLE (63629-2611-1) 20 tablet 2025-04-08 0000-00-00 No No Current 63629-2611-2 63629261102 30 TABLET in 1 BOTTLE (63629-2611-2) 30 tablet 2025-04-08 0000-00-00 No No Current 63629-2611-3 63629261103 60 TABLET in 1 BOTTLE (63629-2611-3) 60 tablet 2025-04-08 0000-00-00 No No Current