Home NDC 71335-1036 Oxycodone and Acetaminophen
Product NDC 71335-1036
11-digit product format 713351036
Labeler code 71335
Product ID 71335-1036_f489795a-878e-4059-b884-f929981061b5
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Oxycodone and Acetaminophen
Dosage form TABLET
Route ORAL
Labeler Bryant Ranch Prepack
Application ANDA201972
Marketing category ANDA
Marketing start 2013-07-15
Substance OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN
Active strength 10; 325 mg/1; mg/1
Pharmacologic classes Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA schedule CII
NDC exclude flag No
Listing certified through 2026-12-31
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 · 40 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 A201972-001 OXYCODONE AND ACETAMINOPHEN ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325MG;2.5MG TABLET / ORAL AA 2013-07-15 A201972-002 OXYCODONE AND ACETAMINOPHEN ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325MG;5MG TABLET / ORAL AA 2013-07-15 A201972-003 OXYCODONE AND ACETAMINOPHEN ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325MG;7.5MG TABLET / ORAL AA 2013-07-15 A201972-004 OXYCODONE AND ACETAMINOPHEN ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325MG;10MG TABLET / ORAL AA 2013-07-15
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 A201972-001 OXYCODONE AND ACETAMINOPHEN 325MG;2.5MG TABLET / ORAL AA 2013-07-15 84e616aacf4f…2026-09-14 22:38:34 2026-08 A201972-002 OXYCODONE AND ACETAMINOPHEN 325MG;5MG TABLET / ORAL AA 2013-07-15 84e616aacf4f…2026-09-14 22:38:34 2026-08 A201972-003 OXYCODONE AND ACETAMINOPHEN 325MG;7.5MG TABLET / ORAL AA 2013-07-15 84e616aacf4f…2026-09-14 22:38:34 2026-08 A201972-004 OXYCODONE AND ACETAMINOPHEN 325MG;10MG TABLET / ORAL AA 2013-07-15 84e616aacf4f…2026-08-18 06:07:40 2026-07 A201972-001 OXYCODONE AND ACETAMINOPHEN 325MG;2.5MG TABLET / ORAL AA 2013-07-15 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A201972-002 OXYCODONE AND ACETAMINOPHEN 325MG;5MG TABLET / ORAL AA 2013-07-15 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A201972-003 OXYCODONE AND ACETAMINOPHEN 325MG;7.5MG TABLET / ORAL AA 2013-07-15 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A201972-004 OXYCODONE AND ACETAMINOPHEN 325MG;10MG TABLET / ORAL AA 2013-07-15 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A201972-001 OXYCODONE AND ACETAMINOPHEN 325MG;2.5MG TABLET / ORAL AA 2013-07-15 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A201972-002 OXYCODONE AND ACETAMINOPHEN 325MG;5MG TABLET / ORAL AA 2013-07-15 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A201972-003 OXYCODONE AND ACETAMINOPHEN 325MG;7.5MG TABLET / ORAL AA 2013-07-15 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A201972-004 OXYCODONE AND ACETAMINOPHEN 325MG;10MG TABLET / ORAL AA 2013-07-15 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A201972-001 OXYCODONE AND ACETAMINOPHEN 325MG;2.5MG TABLET / ORAL AA 2013-07-15 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A201972-002 OXYCODONE AND ACETAMINOPHEN 325MG;5MG TABLET / ORAL AA 2013-07-15 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A201972-003 OXYCODONE AND ACETAMINOPHEN 325MG;7.5MG TABLET / ORAL AA 2013-07-15 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A201972-004 OXYCODONE AND ACETAMINOPHEN 325MG;10MG TABLET / ORAL AA 2013-07-15 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A201972-001 OXYCODONE AND ACETAMINOPHEN 325MG;2.5MG TABLET / ORAL AA 2013-07-15 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A201972-002 OXYCODONE AND ACETAMINOPHEN 325MG;5MG TABLET / ORAL AA 2013-07-15 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A201972-003 OXYCODONE AND ACETAMINOPHEN 325MG;7.5MG TABLET / ORAL AA 2013-07-15 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A201972-004 OXYCODONE AND ACETAMINOPHEN 325MG;10MG TABLET / ORAL AA 2013-07-15 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A201972-001 OXYCODONE AND ACETAMINOPHEN 325MG;2.5MG TABLET / ORAL AA 2013-07-15 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A201972-002 OXYCODONE AND ACETAMINOPHEN 325MG;5MG TABLET / ORAL AA 2013-07-15 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A201972-003 OXYCODONE AND ACETAMINOPHEN 325MG;7.5MG TABLET / ORAL AA 2013-07-15 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A201972-004 OXYCODONE AND ACETAMINOPHEN 325MG;10MG TABLET / ORAL AA 2013-07-15 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A201972-001 OXYCODONE AND ACETAMINOPHEN 325MG;2.5MG TABLET / ORAL AA 2013-07-15 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A201972-002 OXYCODONE AND ACETAMINOPHEN 325MG;5MG TABLET / ORAL AA 2013-07-15 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A201972-003 OXYCODONE AND ACETAMINOPHEN 325MG;7.5MG TABLET / ORAL AA 2013-07-15 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A201972-004 OXYCODONE AND ACETAMINOPHEN 325MG;10MG TABLET / ORAL AA 2013-07-15 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A201972-001 OXYCODONE AND ACETAMINOPHEN 325MG;2.5MG TABLET / ORAL AA 2013-07-15 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A201972-002 OXYCODONE AND ACETAMINOPHEN 325MG;5MG TABLET / ORAL AA 2013-07-15 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A201972-003 OXYCODONE AND ACETAMINOPHEN 325MG;7.5MG TABLET / ORAL AA 2013-07-15 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A201972-004 OXYCODONE AND ACETAMINOPHEN 325MG;10MG TABLET / ORAL AA 2013-07-15 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A201972-001 OXYCODONE AND ACETAMINOPHEN 325MG;2.5MG TABLET / ORAL AA 2013-07-15 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A201972-002 OXYCODONE AND ACETAMINOPHEN 325MG;5MG TABLET / ORAL AA 2013-07-15 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A201972-003 OXYCODONE AND ACETAMINOPHEN 325MG;7.5MG TABLET / ORAL AA 2013-07-15 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A201972-004 OXYCODONE AND ACETAMINOPHEN 325MG;10MG TABLET / ORAL AA 2013-07-15 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A201972-001 OXYCODONE AND ACETAMINOPHEN 325MG;2.5MG TABLET / ORAL AA 2013-07-15 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A201972-002 OXYCODONE AND ACETAMINOPHEN 325MG;5MG TABLET / ORAL AA 2013-07-15 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A201972-003 OXYCODONE AND ACETAMINOPHEN 325MG;7.5MG TABLET / ORAL AA 2013-07-15 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A201972-004 OXYCODONE AND ACETAMINOPHEN 325MG;10MG TABLET / ORAL AA 2013-07-15 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 Oxycodone and Acetaminophen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OXYCODONE HYDROCHLORIDE 10 mg/1 ACETAMINOPHEN 325 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination C1ENJ2TE6C Internal UNII lookup 362O9ITL9D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1049214 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# NDC, Effective, Related label table NDC Effective Related label 71335-1036-1 2024-08-21 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-2 2024-08-21 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-3 2024-08-21 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-4 2024-08-21 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-5 2024-08-21 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-6 2024-08-21 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-7 2024-08-21 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-8 2024-08-21 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-9 2024-08-21 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-1 2024-01-30 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-2 2024-01-30 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-3 2024-01-30 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-4 2024-01-30 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-5 2024-01-30 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-6 2024-01-30 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-7 2024-01-30 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-8 2024-01-30 Oxycodone and Acetaminophen Tablets, USP CII 71335-1036-9 2024-01-30 Oxycodone and Acetaminophen Tablets, USP CII
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71335-1036-1 Oxycodone and Acetaminophen 30 in 1 BOTTLE TABLET 30 4 71335-1036-2 Oxycodone and Acetaminophen 120 in 1 BOTTLE TABLET 120 4 71335-1036-3 Oxycodone and Acetaminophen 90 in 1 BOTTLE TABLET 90 4 71335-1036-4 Oxycodone and Acetaminophen 28 in 1 BOTTLE TABLET 28 4 71335-1036-5 Oxycodone and Acetaminophen 60 in 1 BOTTLE TABLET 60 4 71335-1036-6 Oxycodone and Acetaminophen 20 in 1 BOTTLE TABLET 20 4 71335-1036-7 Oxycodone and Acetaminophen 45 in 1 BOTTLE TABLET 45 4 71335-1036-8 Oxycodone and Acetaminophen 75 in 1 BOTTLE TABLET 75 4 71335-1036-9 Oxycodone and Acetaminophen 100 in 1 BOTTLE TABLET 100 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71335-1036 OXYCODONE AND ACETAMINOPHEN TABLET [BRYANT RANCH PREPACK] 4 Current NDC, Legacy NDC, 9 package rows 20240823_c12c26be-ba05-4d25-a2bf-f87623c6ae57.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 · 4 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Oxycodone and Acetaminophen OXYCODONE AND ACETAMINOPHEN Aurolife Pharma, LLC 69df20d9-b1d5-47dc-9ff0-29987284f8c7 2025-12-23 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 201972 application number: ANDA201972 Oxycodone and Acetaminophen OXYCODONE AND ACETAMINOPHEN Bryant Ranch Prepack c12c26be-ba05-4d25-a2bf-f87623c6ae57 2024-08-09 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 201972 application number: ANDA201972 ndc (product): 71335-1036 Oxycodone and Acetaminophen OXYCODONE AND ACETAMINOPHEN Proficient Rx LP dd4dbe5b-8d07-4a96-a78d-2f20da761dad 2019-11-01 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 201972 application number: ANDA201972 Oxycodone and Acetaminophen OXYCODONE AND ACETAMINOPHEN Proficient Rx LP df97ea5a-51df-453b-b1b4-edc74c718ee7 2019-10-01 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 201972 application number: ANDA201972
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 71335-1036-1 71335103601 30 TABLET in 1 BOTTLE (71335-1036-1) 30 tablet 2019-01-07 0000-00-00 No No Current 71335-1036-2 71335103602 120 TABLET in 1 BOTTLE (71335-1036-2) 120 tablet 2024-08-09 0000-00-00 No No Current 71335-1036-3 71335103603 90 TABLET in 1 BOTTLE (71335-1036-3) 90 tablet 2018-12-24 0000-00-00 No No Current 71335-1036-4 71335103604 28 TABLET in 1 BOTTLE (71335-1036-4) 28 tablet 2024-08-09 0000-00-00 No No Current 71335-1036-5 71335103605 60 TABLET in 1 BOTTLE (71335-1036-5) 60 tablet 2018-12-24 0000-00-00 No No Current 71335-1036-6 71335103606 20 TABLET in 1 BOTTLE (71335-1036-6) 20 tablet 2024-08-09 0000-00-00 No No Current 71335-1036-7 71335103607 45 TABLET in 1 BOTTLE (71335-1036-7) 45 tablet 2024-08-09 0000-00-00 No No Current 71335-1036-8 71335103608 75 TABLET in 1 BOTTLE (71335-1036-8) 75 tablet 2024-08-09 0000-00-00 No No Current 71335-1036-9 71335103609 100 TABLET in 1 BOTTLE (71335-1036-9) 100 tablet 2024-08-09 0000-00-00 No No Current