FDA.reportPublic FDA data

Nortriptyline Hydrochloride

Product NDC
60687-911
11-digit product format
606870911
Labeler code
60687
Product ID
60687-911_44e5c7ee-ebf1-485a-e063-6294a90acb29
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nortriptyline Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
American Health Packaging
Application
ANDA074132
Marketing category
ANDA
Marketing start
2025-12-01
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-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A074132-001NORTRIPTYLINE HYDROCHLORIDENORTRIPTYLINE HYDROCHLORIDEEQ 10MG BASECAPSULE / ORALAB1995-03-27
A074132-002NORTRIPTYLINE HYDROCHLORIDENORTRIPTYLINE HYDROCHLORIDEEQ 25MG BASECAPSULE / ORALAB1995-03-27
A074132-003NORTRIPTYLINE HYDROCHLORIDENORTRIPTYLINE HYDROCHLORIDEEQ 50MG BASECAPSULE / ORALAB1995-03-27
A074132-004NORTRIPTYLINE HYDROCHLORIDENORTRIPTYLINE HYDROCHLORIDEEQ 75MG BASECAPSULE / ORALABRS1995-03-27

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 4 matching rows.

Application-product, TE code table
Application-productTE code
A074132-001AB
A074132-002AB
A074132-003AB
A074132-004AB

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
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-08-01 22:54:322026-06A074132-001NORTRIPTYLINE HYDROCHLORIDEEQ 10MG BASECAPSULE / ORALAB1995-03-27a50c72e98297…
2026-08-01 22:54:322026-06A074132-002NORTRIPTYLINE HYDROCHLORIDEEQ 25MG BASECAPSULE / ORALAB1995-03-27a50c72e98297…
2026-08-01 22:54:322026-06A074132-003NORTRIPTYLINE HYDROCHLORIDEEQ 50MG BASECAPSULE / ORALAB1995-03-27a50c72e98297…
2026-08-01 22:54:322026-06A074132-004NORTRIPTYLINE HYDROCHLORIDEEQ 75MG BASECAPSULE / ORALABRS1995-03-27a50c72e98297…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-08-01 22:54:322026-06A074132-001AB1a50c72e98297…
2026-08-01 22:54:322026-06A074132-002AB1a50c72e98297…
2026-08-01 22:54:322026-06A074132-003AB1a50c72e98297…
2026-08-01 22:54:322026-06A074132-004AB1a50c72e98297…

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 · 17 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEREMEDYREPACK INC.dd1f4d6f-14cc-44c0-b9d3-bb3d17b557fa2026-06-12Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEREMEDYREPACK INC.522d0cd8-d84d-4961-a525-4527fce44c3c2026-06-10Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEA-S Medication Solutionsa2cf7783-7019-49ea-ab55-796674d945462026-03-24Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEBryant Ranch Prepack8eef261f-5c78-a88f-37c4-46e6b0e0f0ee2026-03-10Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDECoupler LLC4c21abdb-f3e9-9037-e063-6294a90af4b42026-03-03Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
NORTRIPTYLINE HYDROCHLORIDENORTRIPTYLINE HYDROCHLORIDEDirect Rx017f7717-e160-4142-9a5a-1a2bd97767072026-01-13Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEAmerican Health Packagingd111c36d-98ed-4f0d-97ea-86fe9048deee2025-12-01Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
ndc (product): 60687-911
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEA-S Medication Solutions686d15d0-6434-42ec-8c78-f45d617d294c2025-12-01Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEBryant Ranch Prepack962f3f54-0556-4509-a231-ca62cb01bec82025-11-17Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEBryant Ranch Prepack43a81887-42b8-43b5-b58a-3f3df2e9949b2025-11-07Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDETeva Pharmaceuticals USA, Inc.b58d473a-b19f-4d2a-b1ae-dd398d7a29e12025-09-30Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEPreferred Pharmaceuticals Inc.af950b46-07df-4de6-a221-d3d7059b87a12025-08-28Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEProficient Rx LPe047f990-c374-4f8f-8583-c615f92545e22024-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEProficient Rx LP2f9fc7a0-163a-4a05-84a7-7999a41ecb1f2024-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEProficient Rx LPb387ba49-fd3f-4488-86e8-9b81e85ab2322024-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEAphena Pharma Solutions - Tennessee, LLCf1868790-c70b-4979-974d-3ce0ffe99e362024-02-01Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132
Nortriptyline HydrochlorideNORTRIPTYLINE HYDROCHLORIDEProficient Rx LP30263e15-de21-4db4-aceb-59d619909e822023-03-01Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 074132
application number: ANDA074132

Additional Listing Data#

Finished product
Yes
Brand name base
Nortriptyline Hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
NORTRIPTYLINE HYDROCHLORIDE25 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
00FN6IH15DInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
198045Internal RxNorm lookup
317136Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
d111c36d-98ed-4f0d-97ea-86fe9048deeeAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
de76de11-1019-6138-2d8a-16fa566ae22aProduct name220241009
53e88688-54e1-9681-22b8-e499bd715088Product name220210729

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60687-911-01Nortriptyline Hydrochloride100 in 1 CARTONCAPSULE1001
60687-911-11Nortriptyline Hydrochloride1 in 1 BLISTER PACKCAPSULE11

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60687-911-01EA - Each60687-9110916b1b1-38c5-4699-ad9c-fe039ab2510012025-12-16
60687-911-11EA - Each60687-911fd6fa1db-cd77-4911-a1f5-5fdefb27dbea12025-12-16

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198045nortriptyline HCl 10 MG Oral CapsulePSNd111c36d-98ed-4f0d-97ea-86fe9048deee1
317136nortriptyline HCl 25 MG Oral CapsulePSNd111c36d-98ed-4f0d-97ea-86fe9048deee1
198045nortriptyline 10 MG Oral CapsuleSCDd111c36d-98ed-4f0d-97ea-86fe9048deee1
317136nortriptyline 25 MG Oral CapsuleSCDd111c36d-98ed-4f0d-97ea-86fe9048deee1
198045nortriptyline (as nortriptyline HCl) 10 MG Oral CapsuleSYd111c36d-98ed-4f0d-97ea-86fe9048deee1
317136nortriptyline (as nortriptyline HCl) 25 MG Oral CapsuleSYd111c36d-98ed-4f0d-97ea-86fe9048deee1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
60687-911-0160687091101100 BLISTER PACK in 1 CARTON (60687-911-01) / 1 CAPSULE in 1 BLISTER PACK (60687-911-11) 100 blister pack2025-12-01NoNoCurrent
60687-911-11606870911111 in 1 BLISTER PACKHistorical