NDC 0037-8120-01 - MUSE
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 0037-8120
- Requested NDC
- 0037-8120-01
- Package NDCs from labels
- 0037-8120-01, 0037-8120-06, 0037-8120-56
- Manufacturer
- Meda Pharmaceuticals Inc.
- Effective date
- 2024-05-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| MUSE ® (alprostadil) urethral suppository | Meda Pharmaceuticals Inc. | 2024-05-15 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0037-8120-06 | 2024-01-30 | C162847 | 48780-1 | 1030e365-29df-111a-e063-dadaa90a10e2 | MUSE ® (alprostadil) urethral suppository |
| 0037-8120-56 | 2024-01-30 | C162847 | 48780-1 | 1030e365-29df-111a-e063-dadaa90a10e2 | MUSE ® (alprostadil) urethral suppository |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0037-8120-01 | EA - Each | 0037-8120 | 679f1c9b-be34-411e-8f90-0c1828ec5945 | 1 | 2012-07-24 |
| 0037-8120-06 | EA - Each | 0037-8120 | 73d8e553-2ede-4737-86ef-5ccca7835271 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Alprostadil | ACTIVE INGREDIENT | F5TD010360 | MUSE (ALPROSTADIL) SUPPOSITORY [MEDA PHARMACEUTICALS INC.] | 10 | |
| Alprostadil | ACTIVE MOIETY | F5TD010360 | MUSE (ALPROSTADIL) SUPPOSITORY [MEDA PHARMACEUTICALS INC.] | 10 | |
| Polyethylene Glycol 1450 | INACTIVE INGREDIENT | OJ4Z5Z32L4 | MUSE (ALPROSTADIL) SUPPOSITORY [MEDA PHARMACEUTICALS INC.] | 10 |
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 |
|---|---|---|---|---|---|---|
| PROSTIN VR PEDIATRIC | ALPROSTADIL | Pharmacia & Upjohn Company LLC | 930f8c02-46a8-4cff-a484-660468ab23c3 | 2026-08-17 | Boxed warning, Warnings, Adverse reactions | F5TD010360 |
| PROSTIN VR PEDIATRIC | ALPROSTADIL | Pharmacia & Upjohn Company LLC | dea460fa-d05e-4191-8461-f185a711ad89 | 2026-08-17 | Boxed warning, Warnings, Adverse reactions | F5TD010360 |
| Alprostadil | ALPROSTADIL | Meitheal Pharmaceuticals Inc. | 35d229e1-6947-435c-bf54-bfa09cca7e53 | 2024-06-04 | Boxed warning, Warnings, Adverse reactions | F5TD010360 |
| e87110b4-64f2-4971-a539-7151c7a3fa21 | 4c55f3f9-c4cf-11df-851a-0800200c9a66 | 2024-05-15 | Warnings, Adverse reactions | 4c55f3f9-c4cf-11df-851a-0800200c9a66 | ||
| Caverject | ALPROSTADIL | Pharmacia & Upjohn Company LLC | a295fc1e-d82c-4f44-bc2d-a552bf594c98 | 2024-05-13 | Warnings, Adverse reactions | F5TD010360 |
| Edex | ALPROSTADIL | Endo USA, Inc. | e8b8ec8d-1318-43e4-a182-446e9f9579de | 2024-03-27 | Warnings, Adverse reactions | F5TD010360 |
| Caverject Impulse | ALPROSTADIL | Pharmacia & Upjohn Company LLC | 4dec1dbd-c63b-4a1b-81cb-c8d29696cc40 | 2024-02-29 | Warnings, Adverse reactions | F5TD010360 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.