Home NDC 70710-1154 Nortriptyline Hydrochloride
Product NDC 70710-1154
11-digit product format 707101154
Labeler code 70710
Product ID 70710-1154_eb495cd8-4bb8-40f5-b578-5e5b9d49b772
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Nortriptyline Hydrochloride
Dosage form CAPSULE
Route ORAL
Labeler Zydus Pharmaceuticals (USA) Inc.
Application ANDA213441
Marketing category ANDA
Marketing start 2022-02-10
Substance NORTRIPTYLINE HYDROCHLORIDE
Active strength 25 mg/1
Pharmacologic classes Tricyclic Antidepressant [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 · 4 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A213441-001 NORTRIPTYLINE HYDROCHLORIDE NORTRIPTYLINE HYDROCHLORIDE EQ 10MG BASE CAPSULE / ORAL 2021-02-24 A213441-002 NORTRIPTYLINE HYDROCHLORIDE NORTRIPTYLINE HYDROCHLORIDE EQ 25MG BASE CAPSULE / ORAL 2021-02-24 A213441-003 NORTRIPTYLINE HYDROCHLORIDE NORTRIPTYLINE HYDROCHLORIDE EQ 50MG BASE CAPSULE / ORAL 2021-02-24 A213441-004 NORTRIPTYLINE HYDROCHLORIDE NORTRIPTYLINE HYDROCHLORIDE EQ 75MG BASE CAPSULE / ORAL 2021-02-24
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 A213441-001 NORTRIPTYLINE HYDROCHLORIDE EQ 10MG BASE CAPSULE / ORAL 2021-02-24 a50c72e98297…2026-08-01 22:54:32 2026-06 A213441-002 NORTRIPTYLINE HYDROCHLORIDE EQ 25MG BASE CAPSULE / ORAL 2021-02-24 a50c72e98297…2026-08-01 22:54:32 2026-06 A213441-003 NORTRIPTYLINE HYDROCHLORIDE EQ 50MG BASE CAPSULE / ORAL 2021-02-24 a50c72e98297…2026-08-01 22:54:32 2026-06 A213441-004 NORTRIPTYLINE HYDROCHLORIDE EQ 75MG BASE CAPSULE / ORAL 2021-02-24 a50c72e98297…
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.
Additional Listing Data#
Finished product Yes
Brand name base Nortriptyline Hydrochloride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength NORTRIPTYLINE HYDROCHLORIDE 25 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 00FN6IH15D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 4 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198045 Internal RxNorm lookup 198046 Internal RxNorm lookup 198047 Internal RxNorm lookup 317136 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 70710-1154-1 Nortriptyline Hydrochloride 100 in 1 BOTTLE CAPSULE 100 2 70710-1154-3 Nortriptyline Hydrochloride 30 in 1 BOTTLE CAPSULE 30 2 70710-1154-5 Nortriptyline Hydrochloride 500 in 1 BOTTLE CAPSULE 500 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70710-1154 NORTRIPTYLINE HYDROCHLORIDE CAPSULE [ZYDUS PHARMACEUTICALS (USA) INC.] 2 Current NDC, Legacy NDC, 3 package rows 20240328_dbe85bdc-17a1-4201-bf48-a52e35d69b68.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 70710-1154-1 70710115401 100 CAPSULE in 1 BOTTLE (70710-1154-1) 100 capsule 2022-02-10 0000-00-00 No No Current 70710-1154-3 70710115403 30 CAPSULE in 1 BOTTLE (70710-1154-3) 30 capsule 2022-02-10 0000-00-00 No No Current 70710-1154-5 70710115405 500 CAPSULE in 1 BOTTLE (70710-1154-5) 500 capsule 2022-02-10 0000-00-00 No No Current