Details for New Drug Application (NDA): 019970
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NDA 019970 describes NITROGLYCERIN IN DEXTROSE 5%, which is a drug marketed by Baxter Hlthcare and Hospira and is included in five NDAs. It is available from two suppliers. Additional details are available on the NITROGLYCERIN IN DEXTROSE 5% profile page.
The generic ingredient in NITROGLYCERIN IN DEXTROSE 5% is nitroglycerin. There are thirty-six drug master file entries for this compound. Thirty-five suppliers are listed for this compound. Additional details are available on the nitroglycerin profile page.
The generic ingredient in NITROGLYCERIN IN DEXTROSE 5% is nitroglycerin. There are thirty-six drug master file entries for this compound. Thirty-five suppliers are listed for this compound. Additional details are available on the nitroglycerin profile page.
Summary for 019970
| Tradename: | NITROGLYCERIN IN DEXTROSE 5% |
| Applicant: | Baxter Hlthcare |
| Ingredient: | nitroglycerin |
| Patents: | 0 |
Pharmacology for NDA: 019970
| Physiological Effect | Vasodilation |
Medical Subject Heading (MeSH) Categories for 019970
Suppliers and Packaging for NDA: 019970
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| NITROGLYCERIN IN DEXTROSE 5% | nitroglycerin | INJECTABLE;INJECTION | 019970 | NDA | Baxter Healthcare Company | 0338-1047 | 0338-1047-02 | 12 BOTTLE, GLASS in 1 BOX (0338-1047-02) / 250 mL in 1 BOTTLE, GLASS |
| NITROGLYCERIN IN DEXTROSE 5% | nitroglycerin | INJECTABLE;INJECTION | 019970 | NDA | Baxter Healthcare Company | 0338-1049 | 0338-1049-02 | 12 BOTTLE, GLASS in 1 BOX (0338-1049-02) / 250 mL in 1 BOTTLE, GLASS |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 10MG/100ML | ||||
| Approval Date: | Dec 29, 1989 | TE: | RLD: | Yes | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 20MG/100ML | ||||
| Approval Date: | Dec 29, 1989 | TE: | RLD: | Yes | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 40MG/100ML | ||||
| Approval Date: | Dec 29, 1989 | TE: | RLD: | Yes | |||||
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