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PROGESTERONE
PROGESTERONE - 0591-3128-79 - (PROGESTERONE)
Drug Information of PROGESTERONE
| Product NDC: | 0591-3128 |
| Proprietary Name: | PROGESTERONE |
| Non Proprietary Name: | PROGESTERONE |
| Active Ingredient(s): | 50 mg/mL & nbsp; PROGESTERONE |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PROGESTERONE
| Product NDC: | 0591-3128 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017362 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19780511 |
Package Information of PROGESTERONE
| Package NDC: | 0591-3128-79 |
| Package Description: | 10 mL in 1 VIAL, MULTI-DOSE (0591-3128-79) |
NDC Information of PROGESTERONE
| NDC Code | 0591-3128-79 |
| Proprietary Name | PROGESTERONE |
| Package Description | 10 mL in 1 VIAL, MULTI-DOSE (0591-3128-79) |
| Product NDC | 0591-3128 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PROGESTERONE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 19780511 |
| Marketing Category Name | NDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | PROGESTERONE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Progesterone [Chemical/Ingredient],Progesterone [EPC] |
