Home NDC 82804-298 Tramadol Hydrochloride
Product NDC 82804-298
11-digit product format 828040298
Labeler code 82804
Product ID 82804-298_aefc85bc-0820-4aee-8d94-313c5f1658f5
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Tramadol Hydrochloride
Dosage form TABLET, FILM COATED, EXTENDED RELEASE
Route ORAL
Labeler Proficient Rx LP
Application ANDA209404
Marketing category ANDA
Marketing start 2025-01-31
Substance TRAMADOL HYDROCHLORIDE
Active strength 100 mg/1
Pharmacologic classes Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA schedule CIV
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
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 A209404-001 TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE 100MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 A209404-002 TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE 200MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 A209404-003 TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE 300MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31
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 2026-09-14 22:38:34 2026-08 A209404-001 TRAMADOL HYDROCHLORIDE 100MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 84e616aacf4f…2026-09-14 22:38:34 2026-08 A209404-002 TRAMADOL HYDROCHLORIDE 200MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 84e616aacf4f…2026-09-14 22:38:34 2026-08 A209404-003 TRAMADOL HYDROCHLORIDE 300MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 84e616aacf4f…2026-08-18 06:07:40 2026-07 A209404-001 TRAMADOL HYDROCHLORIDE 100MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A209404-002 TRAMADOL HYDROCHLORIDE 200MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A209404-003 TRAMADOL HYDROCHLORIDE 300MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A209404-001 TRAMADOL HYDROCHLORIDE 100MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A209404-002 TRAMADOL HYDROCHLORIDE 200MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A209404-003 TRAMADOL HYDROCHLORIDE 300MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A209404-001 TRAMADOL HYDROCHLORIDE 100MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A209404-002 TRAMADOL HYDROCHLORIDE 200MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A209404-003 TRAMADOL HYDROCHLORIDE 300MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A209404-001 TRAMADOL HYDROCHLORIDE 100MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A209404-002 TRAMADOL HYDROCHLORIDE 200MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A209404-003 TRAMADOL HYDROCHLORIDE 300MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A209404-001 TRAMADOL HYDROCHLORIDE 100MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A209404-002 TRAMADOL HYDROCHLORIDE 200MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A209404-003 TRAMADOL HYDROCHLORIDE 300MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A209404-001 TRAMADOL HYDROCHLORIDE 100MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A209404-002 TRAMADOL HYDROCHLORIDE 200MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A209404-003 TRAMADOL HYDROCHLORIDE 300MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 b8a1b40f171c…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A209404-001 TRAMADOL HYDROCHLORIDE 100MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A209404-002 TRAMADOL HYDROCHLORIDE 200MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A209404-003 TRAMADOL HYDROCHLORIDE 300MG TABLET, EXTENDED RELEASE / ORAL AB1 2025-01-31 a50c72e98297…
Observed Orange Book normalized TE history# 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 Tramadol Hydrochloride
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TRAMADOL HYDROCHLORIDE 100 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9N7R477WCK Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 833709 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 · 2 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 82804-298-30 82804029830 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82804-298-30) 2025-01-31 No No Current