Home Applications 083246 Application 083246
Type ANDA
Sponsor OAK PHARMS Application Products# Product, Drug, Ingredient table Product Drug Ingredient Form Strength Reference drug Reference standard 001 NEMBUTAL SODIUM PENTOBARBITAL SODIUM INJECTABLE;INJECTION 50MG/ML No Yes
Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A083246-001 NEMBUTAL SODIUM PENTOBARBITAL SODIUM 50MG/ML INJECTABLE / INJECTION AP RLD, RS, Approved before 1982
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code A083246-001 AP
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 2 of 2 · 43 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 2022-09-29 23:25 UTC 2022-09 A083246-001 NEMBUTAL SODIUM 50MG/ML INJECTABLE / INJECTION AP RLD, RS, Approved before 1982 e64feba35796…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A083246-001 NEMBUTAL SODIUM 50MG/ML INJECTABLE / INJECTION AP RLD, RS, Approved before 1982 cb3db0bc1861…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A083246-001 NEMBUTAL SODIUM 50MG/ML INJECTABLE / INJECTION AP RLD, RS, Approved before 1982 a50c72e98297…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 2 · 43 observed states.
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 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
NDC Listings For This Application# NDC listings for this application page 1 of 1 · 13 matching rows.
NDC, Name, Nonproprietary name table NDC Name Nonproprietary name Labeler Marketing category Status 17478-181 Pentobarbital Sodium Pentobarbital Sodium Akorn, Inc. ANDA Current 17478-181 Pentobarbital Sodium Pentobarbital Sodium Akorn ANDA Current 17478-181 Pentobarbital Sodium Pentobarbital Sodium Akorn ANDA Current 17478-181 Pentobarbital Sodium Pentobarbital Sodium Akorn, Inc. ANDA Current 17478-181 Pentobarbital Sodium Pentobarbital Sodium Akorn, Inc. ANDA Current 17478-181 Pentobarbital Sodium Pentobarbital Sodium Akorn, Inc. ANDA Current 17478-181 Pentobarbital Sodium Pentobarbital Sodium Akorn ANDA Current 76478-501 Nembutal Sodium pentobarbital sodium Akron ANDA Current 76478-501 Nembutal Sodium pentobarbital sodium Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) ANDA Current 76478-501 Nembutal Sodium pentobarbital sodium Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) ANDA Current 76478-501 Nembutal Sodium pentobarbital sodium Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) ANDA Current 76478-501 Nembutal Sodium pentobarbital sodium Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) ANDA Current 76478-501 Nembutal Sodium pentobarbital sodium Akron ANDA Current