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Synarel
Synarel - 0025-0166-08 - (nafarelin acetate)
Drug Information of Synarel
| Product NDC: | 0025-0166 |
| Proprietary Name: | Synarel |
| Non Proprietary Name: | nafarelin acetate |
| Active Ingredient(s): | 2 mg/mL & nbsp; nafarelin acetate |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Synarel
| Product NDC: | 0025-0166 |
| Labeler Name: | G.D. Searle LLC Division of Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019886 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19900213 |
Package Information of Synarel
| Package NDC: | 0025-0166-08 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (0025-0166-08) > 8 mL in 1 BOTTLE, SPRAY |
NDC Information of Synarel
| NDC Code | 0025-0166-08 |
| Proprietary Name | Synarel |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (0025-0166-08) > 8 mL in 1 BOTTLE, SPRAY |
| Product NDC | 0025-0166 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nafarelin acetate |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 19900213 |
| Marketing Category Name | NDA |
| Labeler Name | G.D. Searle LLC Division of Pfizer Inc |
| Substance Name | NAFARELIN ACETATE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Gonadotropin Releasing Hormone Receptor Agonist [EPC],Gonadotropin Releasing Hormone Receptor Agonists [MoA] |
