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Oxytocin
Oxytocin - 63323-012-10 - (OXYTOCIN)
Drug Information of Oxytocin
| Product NDC: | 63323-012 |
| Proprietary Name: | Oxytocin |
| Non Proprietary Name: | OXYTOCIN |
| Active Ingredient(s): | 10 [USP'U]/mL & nbsp; OXYTOCIN |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxytocin
| Product NDC: | 63323-012 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018248 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000810 |
Package Information of Oxytocin
| Package NDC: | 63323-012-10 |
| Package Description: | 25 VIAL, MULTI-DOSE in 1 TRAY (63323-012-10) > 10 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Oxytocin
| NDC Code | 63323-012-10 |
| Proprietary Name | Oxytocin |
| Package Description | 25 VIAL, MULTI-DOSE in 1 TRAY (63323-012-10) > 10 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 63323-012 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | OXYTOCIN |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20000810 |
| Marketing Category Name | NDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | OXYTOCIN |
| Strength Number | 10 |
| Strength Unit | [USP'U]/mL |
| Pharmaceutical Classes | Increased Uterine Smooth Muscle Contraction or Tone [PE],Oxytocic [EPC],Oxytocin [Chemical/Ingredient] |
