Home DailyMed 92f2468a-c558-45b2-85a9-8a03cb3f2f21 National Council for Prescription Drug Programs indexing - billing unit Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer National Council for Prescription Drug Programs
Effective date 2012-07-24
Label type Indexing - Billing Unit
Version 1
Source full-release
Hydrated at 2026-06-05 02:15:53
Orange Book application contexts# All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.
Orange Book application contexts page 1 of 1 · 1 matching rows.
Source provenance: Browse the complete Orange Book source catalog · source snapshot 45 .
Orange Book products# Current product rows page 1 of 1 · 8 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N021272-001 REMODULIN TREPROSTINIL 1MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 N021272-002 REMODULIN TREPROSTINIL 2.5MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 N021272-003 REMODULIN TREPROSTINIL 5MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 N021272-004 REMODULIN TREPROSTINIL 10MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 N021272-005 REMODULIN TREPROSTINIL 20MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2021-07-30 N021272-006 REMODULIN TREPROSTINIL 0.1MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2023-09-28 N021272-007 REMODULIN TREPROSTINIL 0.2MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2023-09-28 N021272-008 REMODULIN TREPROSTINIL 0.4MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD, RS 2023-09-28
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 4 matching rows.
Orange Book patents# Current patent rows page 1 of 1 · 40 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.
Product history page 1 of 8 · 286 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 2026-11-14 07:37:17 2026-10 N021272-001 REMODULIN 1MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-002 REMODULIN 2.5MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-003 REMODULIN 5MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-004 REMODULIN 10MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-005 REMODULIN 20MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2021-07-30 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-006 REMODULIN 0.1MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2023-09-28 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-007 REMODULIN 0.2MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2023-09-28 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-008 REMODULIN 0.4MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD, RS 2023-09-28 d4dbc9d85df4…2026-10-15 13:18:30 2026-09 N021272-001 REMODULIN 1MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 c2088c7a36db…2026-10-15 13:18:30 2026-09 N021272-002 REMODULIN 2.5MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 c2088c7a36db…2026-10-15 13:18:30 2026-09 N021272-003 REMODULIN 5MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 c2088c7a36db…2026-10-15 13:18:30 2026-09 N021272-004 REMODULIN 10MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 c2088c7a36db…2026-10-15 13:18:30 2026-09 N021272-005 REMODULIN 20MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2021-07-30 c2088c7a36db…2026-10-15 13:18:30 2026-09 N021272-006 REMODULIN 0.1MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2023-09-28 c2088c7a36db…2026-10-15 13:18:30 2026-09 N021272-007 REMODULIN 0.2MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2023-09-28 c2088c7a36db…2026-10-15 13:18:30 2026-09 N021272-008 REMODULIN 0.4MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD, RS 2023-09-28 c2088c7a36db…2026-09-14 22:38:34 2026-08 N021272-001 REMODULIN 1MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 84e616aacf4f…2026-09-14 22:38:34 2026-08 N021272-002 REMODULIN 2.5MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 84e616aacf4f…2026-09-14 22:38:34 2026-08 N021272-003 REMODULIN 5MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 84e616aacf4f…2026-09-14 22:38:34 2026-08 N021272-004 REMODULIN 10MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 84e616aacf4f…2026-09-14 22:38:34 2026-08 N021272-005 REMODULIN 20MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2021-07-30 84e616aacf4f…2026-09-14 22:38:34 2026-08 N021272-006 REMODULIN 0.1MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2023-09-28 84e616aacf4f…2026-09-14 22:38:34 2026-08 N021272-007 REMODULIN 0.2MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2023-09-28 84e616aacf4f…2026-09-14 22:38:34 2026-08 N021272-008 REMODULIN 0.4MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD, RS 2023-09-28 84e616aacf4f…2026-08-18 06:07:40 2026-07 N021272-001 REMODULIN 1MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N021272-002 REMODULIN 2.5MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N021272-003 REMODULIN 5MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N021272-004 REMODULIN 10MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N021272-005 REMODULIN 20MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2021-07-30 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N021272-006 REMODULIN 0.1MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2023-09-28 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N021272-007 REMODULIN 0.2MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2023-09-28 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N021272-008 REMODULIN 0.4MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD, RS 2023-09-28 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 N021272-001 REMODULIN 1MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021272-002 REMODULIN 2.5MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021272-003 REMODULIN 5MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021272-004 REMODULIN 10MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS AP RLD, RS 2002-05-21 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021272-005 REMODULIN 20MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2021-07-30 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021272-006 REMODULIN 0.1MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2023-09-28 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021272-007 REMODULIN 0.2MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD 2023-09-28 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021272-008 REMODULIN 0.4MG/ML INJECTABLE / INTRAVENOUS, SUBCUTANEOUS RLD, RS 2023-09-28 011fe1cb6892…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 5 · 180 observed states.
Observed Orange Book patent history# Patent history page 1 of 56 · 2,206 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Patent Expiration Use code Coverage / status Submission date Source SHA-256 2026-11-14 07:37:17 2026-10 N021272-001 8653137 2028-09-05 U-1437 2014-02-18 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-001 8658694 2028-09-05 U-1437 2014-02-25 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-001 11723887 2028-12-15 Drug substance 2023-08-15 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-001 9593066 2028-12-15 Drug substance 2017-03-14 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-001 7999007 2029-03-29 U-1437 Drug product 2011-08-23 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-002 8653137 2028-09-05 U-1437 2014-02-18 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-002 8658694 2028-09-05 U-1437 2014-02-25 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-002 11723887 2028-12-15 Drug substance 2023-08-15 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-002 9593066 2028-12-15 Drug substance 2017-03-14 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-002 7999007 2029-03-29 U-1437 Drug product d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-003 8653137 2028-09-05 U-1437 2014-02-18 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-003 8658694 2028-09-05 U-1437 2014-02-25 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-003 11723887 2028-12-15 Drug substance 2023-08-15 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-003 9593066 2028-12-15 Drug substance 2017-03-14 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-003 7999007 2029-03-29 U-1437 Drug product d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-004 8653137 2028-09-05 U-1437 2014-02-18 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-004 8658694 2028-09-05 U-1437 2014-02-25 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-004 11723887 2028-12-15 Drug substance 2023-08-15 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-004 9593066 2028-12-15 Drug substance 2017-03-14 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-004 7999007 2029-03-29 U-1437 Drug product d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-005 8653137 2028-09-05 U-1437 2021-08-24 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-005 8658694 2028-09-05 U-1437 2021-08-24 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-005 11723887 2028-12-15 Drug substance 2023-08-15 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-005 9593066 2028-12-15 Drug substance 2021-08-24 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-005 7999007 2029-03-29 U-1437 Drug product 2021-08-24 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-006 8653137 2028-09-05 U-1437 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-006 8658694 2028-09-05 U-1437 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-006 11723887 2028-12-15 Drug substance 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-006 9593066 2028-12-15 Drug substance 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-006 7999007 2029-03-29 U-1437 Drug product 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-007 8653137 2028-09-05 U-1437 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-007 8658694 2028-09-05 U-1437 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-007 11723887 2028-12-15 Drug substance 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-007 9593066 2028-12-15 Drug substance 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-007 7999007 2029-03-29 U-1437 Drug product 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-008 8653137 2028-09-05 U-1437 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-008 8658694 2028-09-05 U-1437 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-008 11723887 2028-12-15 Drug substance 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-008 9593066 2028-12-15 Drug substance 2023-10-20 d4dbc9d85df4…2026-11-14 07:37:17 2026-10 N021272-008 7999007 2029-03-29 U-1437 Drug product 2023-10-20 d4dbc9d85df4…
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.