Home NDC 67296-1623-1 Hydrocodone Bitartrate and Acetaminophen
Product NDC 67296-1623
Requested package NDC 67296-1623-1
11-digit product format 672961623
Labeler code 67296
Product ID 67296-1623_b8d0796c-80c5-1386-e053-2a95a90a676f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Hydrocodone Bitartrate and Acetaminophen
Dosage form TABLET
Route ORAL
Labeler RedPharm Drug, Inc.
Application ANDA209037
Marketing category ANDA
Marketing start 2018-01-01
Marketing end 0000-00-00
Substance HYDROCODONE BITARTRATE; ACETAMINOPHEN
Active strength 5 mg/1; mg/1
Pharmacologic classes Opioid Agonist [EPC],Opioid Agonists [MoA]
DEA schedule CII
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 3 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A209037-001 HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHEN; HYDROCODONE BITARTRATE 325MG;5MG TABLET / ORAL AA 2017-06-21 A209037-002 HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHEN; HYDROCODONE BITARTRATE 325MG;7.5MG TABLET / ORAL AA 2017-06-21 A209037-003 HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHEN; HYDROCODONE BITARTRATE 325MG;10MG TABLET / ORAL AA 2017-06-21
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 3 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.
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 2026-08-01 22:54:32 2026-06 A209037-001 HYDROCODONE BITARTRATE AND ACETAMINOPHEN 325MG;5MG TABLET / ORAL AA 2017-06-21 a50c72e98297…2026-08-01 22:54:32 2026-06 A209037-002 HYDROCODONE BITARTRATE AND ACETAMINOPHEN 325MG;7.5MG TABLET / ORAL AA 2017-06-21 a50c72e98297…2026-08-01 22:54:32 2026-06 A209037-003 HYDROCODONE BITARTRATE AND ACETAMINOPHEN 325MG;10MG TABLET / ORAL AA 2017-06-21 a50c72e98297…
Observed Orange Book normalized TE history# openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 2 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67296-1623-0 Hydrocodone Bitartrate and Acetaminophen 40 in 1 BOTTLE TABLET 40 14 67296-1623-1 Hydrocodone Bitartrate and Acetaminophen 10 in 1 BOTTLE TABLET 10 14 67296-1623-2 Hydrocodone Bitartrate and Acetaminophen 20 in 1 BOTTLE TABLET 20 14 67296-1623-3 Hydrocodone Bitartrate and Acetaminophen 30 in 1 BOTTLE TABLET 30 14 67296-1623-4 Hydrocodone Bitartrate and Acetaminophen 4 in 1 BOTTLE TABLET 4 14 67296-1623-5 Hydrocodone Bitartrate and Acetaminophen 12 in 1 BOTTLE TABLET 12 14 67296-1623-6 Hydrocodone Bitartrate and Acetaminophen 6 in 1 BOTTLE TABLET 6 14 67296-1623-7 Hydrocodone Bitartrate and Acetaminophen 15 in 1 BOTTLE TABLET 15 14 67296-1623-8 Hydrocodone Bitartrate and Acetaminophen 50 in 1 BOTTLE TABLET 50 14 67296-1623-9 Hydrocodone Bitartrate and Acetaminophen 60 in 1 BOTTLE TABLET 60 14
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67296-1623 HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [REDPHARM DRUG, INC.] 14 Legacy NDC, 10 package rows 20240725_7b24fc1d-6e2f-47f2-e053-2991aa0a01bb.zip
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 67296-1623-1 67296162301 10 TABLET in 1 BOTTLE (67296-1623-1) 10 tablet 2018-01-01 0000-00-00 No No Current