Details for New Drug Application (NDA): 018924
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NDA 018924 describes AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER, which is a drug marketed by Hospira and is included in one NDA. Additional details are available on the AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER profile page.
The generic ingredient in AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER is aminophylline. There are four drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the aminophylline profile page.
The generic ingredient in AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER is aminophylline. There are four drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the aminophylline profile page.
Summary for 018924
| Tradename: | AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER |
| Applicant: | Hospira |
| Ingredient: | aminophylline |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 018924
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | 100MG/100ML | ||||
| Approval Date: | Dec 12, 1984 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | 200MG/100ML | ||||
| Approval Date: | Dec 12, 1984 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | 400MG/100ML | ||||
| Approval Date: | Dec 12, 1984 | TE: | RLD: | No | |||||
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