Liraglutide
- Product NDC
- 0143-9144
- Requested package NDC
- 0143-9144-03
- 11-digit product format
- 001439144
- Labeler code
- 0143
- Product ID
- 0143-9144_4e2acb7a-d32d-49d3-b59b-39332b5809f3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- liraglutide
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA215503
- Marketing category
- ANDA
- Marketing start
- 2024-12-24
- Substance
- LIRAGLUTIDE
- Active strength
- 6 mg/mL
- Pharmacologic classes
- GLP-1 Receptor Agonist [EPC], Glucagon-Like Peptide 1 [CS], Glucagon-like Peptide-1 (GLP-1) Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Orange Book products#
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| A215503-001 | LIRAGLUTIDE | LIRAGLUTIDE | 18MG/3ML (6MG/ML) | SOLUTION / SUBCUTANEOUS | AP1 | 2024-12-23 |
Therapeutic equivalence codes#
| Application-product | TE code |
|---|---|
| A215503-001 | AP1 |
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 | 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 | A215503-001 | LIRAGLUTIDE | 18MG/3ML (6MG/ML) | SOLUTION / SUBCUTANEOUS | AP1 | 2024-12-23 | 84e616aacf4f… | |
| 2026-08-18 06:07:40 | 2026-07 | A215503-001 | LIRAGLUTIDE | 18MG/3ML (6MG/ML) | SOLUTION / SUBCUTANEOUS | AP1 | 2024-12-23 | caaa826d4ba7… | |
| 2026-02-19 14:30 UTC | 2026-02 | A215503-001 | LIRAGLUTIDE | 18MG/3ML (6MG/ML) | SOLUTION / SUBCUTANEOUS | AP1 | 2024-12-23 | 011fe1cb6892… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | A215503-001 | LIRAGLUTIDE | 18MG/3ML (6MG/ML) | SOLUTION / SUBCUTANEOUS | AP1 | 2024-12-23 | 31067a03dcf5… | |
| 2025-08-23 18:47 UTC | 2025-08 | A215503-001 | LIRAGLUTIDE | 18MG/3ML (6MG/ML) | SOLUTION / SUBCUTANEOUS | AP | 2024-12-23 | 6a471c1ec25d… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | A215503-001 | LIRAGLUTIDE | 18MG/3ML (6MG/ML) | SOLUTION / SUBCUTANEOUS | AP | 2024-12-23 | fd3edfee7708… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | A215503-001 | LIRAGLUTIDE | 18MG/3ML (6MG/ML) | SOLUTION / SUBCUTANEOUS | AP | 2024-12-23 | b8a1b40f171c… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | A215503-001 | LIRAGLUTIDE | 18MG/3ML (6MG/ML) | SOLUTION / SUBCUTANEOUS | AP | 2024-12-23 | 03ed91905a0d… | |
| 2026-07-26 02:55 UTC · 3 captures of this ZIP | 2026-06 | A215503-001 | LIRAGLUTIDE | 18MG/3ML (6MG/ML) | SOLUTION / SUBCUTANEOUS | AP1 | 2024-12-23 | a50c72e98297… |
Observed Orange Book normalized TE history#
| Captured | Edition | Application-product | TE code | Order | Source SHA-256 |
|---|---|---|---|---|---|
| 2026-09-14 22:38:34 | 2026-08 | A215503-001 | AP1 | 1 | 84e616aacf4f… |
| 2026-08-18 06:07:40 | 2026-07 | A215503-001 | AP1 | 1 | caaa826d4ba7… |
| 2026-02-19 14:30 UTC | 2026-02 | A215503-001 | AP1 | 1 | 011fe1cb6892… |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | A215503-001 | AP1 | 1 | 31067a03dcf5… |
| 2025-08-23 18:47 UTC | 2025-08 | A215503-001 | AP | 1 | 6a471c1ec25d… |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | A215503-001 | AP | 1 | fd3edfee7708… |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | A215503-001 | AP | 1 | b8a1b40f171c… |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | A215503-001 | AP | 1 | 03ed91905a0d… |
| 2026-07-26 02:55 UTC · 3 captures of this ZIP | 2026-06 | A215503-001 | AP1 | 1 | a50c72e98297… |
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
- Liraglutide
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| LIRAGLUTIDE | 6 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 839I73S42A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 897122 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2100ec49-57b2-4330-ab5f-057ce9b7e4d0 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d8dac6c8-0045-42cf-b357-c3350b4ada5c | Product name | 2 | 20251021 |
| 0dd952e2-ff48-4739-9b8d-72ae0b326834 | Product name | 2 | 20200323 |
| ce962b7e-f9f8-43e6-8d30-41514e79f3e4 | Product name | 1 | 20190201 |
| 2f360a13-6ea8-4c2b-b2ef-10133c2836d9 | Product name | 1 | 20150316 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0143-9144-01 | Liraglutide | 3 mL in 1 SYRINGE, PLASTIC | INJECTION | 3 | 6 | |
| 0143-9144-02 | Liraglutide | 2 in 1 CARTON | INJECTION | 2 | 6 | |
| 0143-9144-03 | Liraglutide | 3 in 1 CARTON | INJECTION | 3 | 6 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0143-9144-01 | ML - Milliliter | 0143-9144 | 8a190f72-c9ff-4b2f-b202-f7bb9ac142bf | 1 | 2026-04-20 |
| 0143-9144-02 | ML - Milliliter | 0143-9144 | 48c7576e-790f-409c-adfe-c0f4c6e091b8 | 1 | 2025-01-14 |
| 0143-9144-03 | ML - Milliliter | 0143-9144 | d973bea9-19c8-413a-95aa-c00afd1105cb | 1 | 2025-01-14 |
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Liraglutide | LIRAGLUTIDE | Hikma Pharmaceuticals USA Inc. | 2100ec49-57b2-4330-ab5f-057ce9b7e4d0 | 2026-05-14 | Boxed warning, Warnings, Adverse reactions | 215503 ANDA215503 0143-9144-03 0143-9144 00143914403 |
| Liraglutide | LIRAGLUTIDE | Hybio Pharmaceutical Co., Ltd. (Pingshan Factory) | 1a372465-d56b-2b80-e063-6394a90a3304 | 2024-12-03 | Warnings, Adverse reactions | 215503 ANDA215503 |
| Liraglutide | LIRAGLUTIDE | Hybio Pharmaceutical Co., Ltd. (Pingshan Factory) | 1a36f43f-d734-97cc-e063-6294a90ae0da | 2024-12-02 | Warnings, Adverse reactions | 215503 ANDA215503 |
| Liraglutide | LIRAGLUTIDE | Hybio Pharmaceutical Co., Ltd. (Pingshan Factory) | 1a36b801-41e2-2eed-e063-6294a90a6f27 | 2024-06-05 | Warnings, Adverse reactions | 215503 ANDA215503 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 897122 | liraglutide 6 MG/ML in 3 ML Pen Injector | PSN | 2100ec49-57b2-4330-ab5f-057ce9b7e4d0 | 6 |
| 897122 | 3 ML liraglutide 6 MG/ML Pen Injector | SCD | 2100ec49-57b2-4330-ab5f-057ce9b7e4d0 | 6 |
| 897122 | liraglutide 18 MG per 3 ML Pen Injector | SY | 2100ec49-57b2-4330-ab5f-057ce9b7e4d0 | 6 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|
| 0143-9144-03 | 00143914403 | 3 SYRINGE, PLASTIC in 1 CARTON (0143-9144-03) / 3 mL in 1 SYRINGE, PLASTIC (0143-9144-01) | 2024-12-24 | No | No | Current |