Details for New Drug Application (NDA): 010942
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NDA 010942 describes SPARINE, which is a drug marketed by Wyeth Ayerst and Hikma and is included in three NDAs. Additional details are available on the SPARINE profile page.
The generic ingredient in SPARINE is promazine hydrochloride. There are thirty-seven drug master file entries for this compound. Additional details are available on the promazine hydrochloride profile page.
The generic ingredient in SPARINE is promazine hydrochloride. There are thirty-seven drug master file entries for this compound. Additional details are available on the promazine hydrochloride profile page.
Summary for 010942
| Tradename: | SPARINE |
| Applicant: | Wyeth Ayerst |
| Ingredient: | promazine hydrochloride |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 010942
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CONCENTRATE;ORAL | Strength | 30MG/ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | SYRUP;ORAL | Strength | 10MG/5ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | No | |||||
Profile for product number 004
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CONCENTRATE;ORAL | Strength | 100MG/ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | No | |||||
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