Details for New Drug Application (NDA): 021671
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The generic ingredient in DEPODUR is morphine sulfate. There are twenty-three drug master file entries for this compound. Twenty-eight suppliers are listed for this compound. Additional details are available on the morphine sulfate profile page.
Summary for 021671
| Tradename: | DEPODUR |
| Applicant: | Pacira Pharms Inc |
| Ingredient: | morphine sulfate |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 021671
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE, LIPOSOMAL;EPIDURAL | Strength | 10MG/ML (10MG/ML) | ||||
| Approval Date: | May 18, 2004 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE, LIPOSOMAL;EPIDURAL | Strength | 15MG/1.5ML (10MG/ML) | ||||
| Approval Date: | May 18, 2004 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE, LIPOSOMAL;EPIDURAL | Strength | 20MG/2ML (10MG/ML) | ||||
| Approval Date: | May 18, 2004 | TE: | RLD: | No | |||||
Expired US Patents for NDA 021671
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
|---|---|---|---|---|---|---|---|
| Pacira Pharms Inc | DEPODUR | morphine sulfate | INJECTABLE, LIPOSOMAL;EPIDURAL | 021671-002 | May 18, 2004 | ⤷ Get Started Free | ⤷ Get Started Free |
| Pacira Pharms Inc | DEPODUR | morphine sulfate | INJECTABLE, LIPOSOMAL;EPIDURAL | 021671-002 | May 18, 2004 | ⤷ Get Started Free | ⤷ Get Started Free |
| Pacira Pharms Inc | DEPODUR | morphine sulfate | INJECTABLE, LIPOSOMAL;EPIDURAL | 021671-001 | May 18, 2004 | ⤷ Get Started Free | ⤷ Get Started Free |
| Pacira Pharms Inc | DEPODUR | morphine sulfate | INJECTABLE, LIPOSOMAL;EPIDURAL | 021671-002 | May 18, 2004 | ⤷ Get Started Free | ⤷ Get Started Free |
| Pacira Pharms Inc | DEPODUR | morphine sulfate | INJECTABLE, LIPOSOMAL;EPIDURAL | 021671-002 | May 18, 2004 | ⤷ Get Started Free | ⤷ Get Started Free |
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
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