Details for New Drug Application (NDA): 050207
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NDA 050207 describes ERYPED, which is a drug marketed by Azurity and is included in two NDAs. It is available from four suppliers. Additional details are available on the ERYPED profile page.
The generic ingredient in ERYPED is erythromycin ethylsuccinate. There are one hundred and three drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the erythromycin ethylsuccinate profile page.
The generic ingredient in ERYPED is erythromycin ethylsuccinate. There are one hundred and three drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the erythromycin ethylsuccinate profile page.
Summary for 050207
| Tradename: | ERYPED |
| Applicant: | Azurity |
| Ingredient: | erythromycin ethylsuccinate |
| Patents: | 0 |
Pharmacology for NDA: 050207
| Physiological Effect | Decreased Sebaceous Gland Activity |
Medical Subject Heading (MeSH) Categories for 050207
Suppliers and Packaging for NDA: 050207
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| E.E.S. | erythromycin ethylsuccinate | GRANULE;ORAL | 050207 | NDA | Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) | 24338-130 | 24338-130-13 | 100 mL in 1 BOTTLE (24338-130-13) |
| E.E.S. | erythromycin ethylsuccinate | GRANULE;ORAL | 050207 | NDA | Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) | 24338-132 | 24338-132-13 | 100 mL in 1 BOTTLE (24338-132-13) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | GRANULE;ORAL | Strength | EQ 200MG BASE/5ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | AB | RLD: | Yes | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | GRANULE;ORAL | Strength | EQ 400MG BASE/5ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | AB | RLD: | Yes | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | GRANULE;ORAL | Strength | EQ 200MG BASE/5ML | ||||
| Approval Date: | Mar 30, 1987 | TE: | AB | RLD: | Yes | ||||
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