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Oxytocin
Oxytocin - 10019-291-02 - (Oxytocin)
Drug Information of Oxytocin
| Product NDC: | 10019-291 |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxytocin
| Product NDC: | 10019-291 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018243 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090626 |
Package Information of Oxytocin
| Package NDC: | 10019-291-02 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 CARTON (10019-291-02) > 1 mL in 1 VIAL, SINGLE-DOSE (10019-291-12) |
NDC Information of Oxytocin
| NDC Code | 10019-291-02 |
| Proprietary Name | Oxytocin |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (10019-291-02) > 1 mL in 1 VIAL, SINGLE-DOSE (10019-291-12) |
| Product NDC | 10019-291 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxytocin |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20090626 |
| Marketing Category Name | NDA |
| Labeler Name | Baxter Healthcare Corporation |
| 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] |
