Home NDC 10370-317 Sitagliptin and Metformin hydrochloride
Product NDC 10370-317
11-digit product format 103700317
Labeler code 10370
Product ID 10370-317_6fd84734-1ea9-46b3-8ca9-0a61340f1390
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name sitagliptin and metformin hydrochloride
Dosage form TABLET, FILM COATED, EXTENDED RELEASE
Route ORAL
Labeler Par Health USA, LLC
Application ANDA204144
Marketing category ANDA
Marketing start 2026-07-24
Substance SITAGLIPTIN PHOSPHATE; METFORMIN HYDROCHLORIDE
Active strength 50; 500 mg/1; mg/1
Pharmacologic classes Biguanide [EPC], Biguanides [CS], Dipeptidyl Peptidase 4 Inhibitor [EPC], Dipeptidyl Peptidase 4 Inhibitors [MoA]
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 A204144-001 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE 500MG;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL AB 2025-06-04 A204144-002 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE 1GM;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL AB 2025-06-04 A204144-003 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE 1GM;EQ 100MG BASE TABLET, EXTENDED RELEASE / ORAL AB 2025-06-04
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 A204144-001 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 500MG;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL AB 2025-06-04 84e616aacf4f…2026-09-14 22:38:34 2026-08 A204144-002 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 1GM;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL AB 2025-06-04 84e616aacf4f…2026-09-14 22:38:34 2026-08 A204144-003 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 1GM;EQ 100MG BASE TABLET, EXTENDED RELEASE / ORAL AB 2025-06-04 84e616aacf4f…2026-08-18 06:07:40 2026-07 A204144-001 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 500MG;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL AB 2025-06-04 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A204144-002 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 1GM;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL AB 2025-06-04 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A204144-003 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 1GM;EQ 100MG BASE TABLET, EXTENDED RELEASE / ORAL AB 2025-06-04 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A204144-001 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 500MG;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL 2025-06-04 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A204144-002 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 1GM;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL 2025-06-04 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A204144-003 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 1GM;EQ 100MG BASE TABLET, EXTENDED RELEASE / ORAL 2025-06-04 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A204144-001 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 500MG;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL 2025-06-04 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A204144-002 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 1GM;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL 2025-06-04 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A204144-003 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 1GM;EQ 100MG BASE TABLET, EXTENDED RELEASE / ORAL 2025-06-04 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A204144-001 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 500MG;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL 2025-06-04 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A204144-002 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 1GM;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL 2025-06-04 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A204144-003 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 1GM;EQ 100MG BASE TABLET, EXTENDED RELEASE / ORAL 2025-06-04 6a471c1ec25d…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A204144-001 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 500MG;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL AB 2025-06-04 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A204144-002 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 1GM;EQ 50MG BASE TABLET, EXTENDED RELEASE / ORAL AB 2025-06-04 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A204144-003 SITAGLIPTIN AND METFORMIN HYDROCHLORIDE 1GM;EQ 100MG BASE TABLET, EXTENDED RELEASE / ORAL AB 2025-06-04 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 Sitagliptin and Metformin hydrochloride
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SITAGLIPTIN PHOSPHATE 50 mg/1 METFORMIN HYDROCHLORIDE 500 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 786Z46389E Internal UNII lookup TS63EW8X6F Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2709470 Internal RxNorm lookup 2709477 Internal RxNorm lookup 2709482 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 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 10370-317-02 10370031702 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (10370-317-02) 2026-07-24 No No Current