Details for New Drug Application (NDA): 206573
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NDA 206573 describes MORPHINE SULFATE, which is a drug marketed by Actavis Elizabeth, Impax Labs Inc, Nortec Dev Assoc, Strides Pharma, Teva Pharms Usa, Upsher Smith Labs, Hikma, Hospira, Hospira Inc, Icu Medical Inc, Intl Medication Sys, Specgx Llc, Watson Labs, Fresenius Kabi Usa, Ani Pharms, Chartwell Molecular, Nostrum Labs Inc, Padagis Us, Pharm Assoc, Rhodes Pharms, Tris Pharma Inc, Vistapharm, Winder Labs Llc, Dava Pharms Inc, Dr Reddys Labs Sa, Epic Pharma Llc, Nesher Pharms, Novel Labs Inc, Rising, Sun Pharm Inds Ltd, Sun Pharm Industries, Alkem Labs Ltd, Ingenus Pharms Nj, and Meridian Medcl Techn, and is included in sixty-two NDAs. It is available from twenty-nine suppliers. There are three patents protecting this drug. Additional details are available on the MORPHINE SULFATE profile page.
The generic ingredient in MORPHINE SULFATE is morphine sulfate. There are twenty-three drug master file entries for this compound. Thirty-one suppliers are listed for this compound. Additional details are available on the morphine sulfate profile page.
The generic ingredient in MORPHINE SULFATE is morphine sulfate. There are twenty-three drug master file entries for this compound. Thirty-one suppliers are listed for this compound. Additional details are available on the morphine sulfate profile page.
Summary for 206573
| Tradename: | MORPHINE SULFATE |
| Applicant: | Pharm Assoc |
| Ingredient: | morphine sulfate |
| Patents: | 0 |
Pharmacology for NDA: 206573
| Mechanism of Action | Full Opioid Agonists |
Medical Subject Heading (MeSH) Categories for 206573
Suppliers and Packaging for NDA: 206573
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| MORPHINE SULFATE | morphine sulfate | SOLUTION;ORAL | 206573 | ANDA | PAI Holdings, LLC dba PAI Pharma | 0121-0825 | 0121-0825-01 | 30 mL in 1 BOTTLE (0121-0825-01) |
| MORPHINE SULFATE | morphine sulfate | SOLUTION;ORAL | 206573 | ANDA | PAI Holdings, LLC dba PAI Pharma | 0121-0825 | 0121-0825-04 | 118 mL in 1 BOTTLE (0121-0825-04) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | SOLUTION;ORAL | Strength | 100MG/5ML | ||||
| Approval Date: | Nov 14, 2016 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | SOLUTION;ORAL | Strength | 10MG/5ML | ||||
| Approval Date: | Sep 12, 2023 | TE: | RLD: | No | |||||
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