progesterone
Generic: progesterone
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
progesterone
Generic Name
progesterone
Labeler
actavis pharma, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
progesterone 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0591-3128
Product ID
0591-3128_aacccc63-aa7d-435e-bec5-0aab0e04153f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA017362
Listing Expiration
2026-12-31
Marketing Start
1978-05-11
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05913128
Hyphenated Format
0591-3128
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
progesterone (source: ndc)
Generic Name
progesterone (source: ndc)
Application Number
NDA017362 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 10 mL in 1 VIAL, MULTI-DOSE (0591-3128-79)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "aacccc63-aa7d-435e-bec5-0aab0e04153f", "openfda": {"nui": ["M0017672", "N0000175601"], "unii": ["4G7DS2Q64Y"], "rxcui": ["312644"], "spl_set_id": ["a09a3b76-36f1-4d20-930e-7e3da97e7ebd"], "pharm_class_cs": ["Progesterone [CS]"], "pharm_class_epc": ["Progesterone [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, MULTI-DOSE (0591-3128-79)", "package_ndc": "0591-3128-79", "marketing_start_date": "19780511"}], "brand_name": "PROGESTERONE", "product_id": "0591-3128_aacccc63-aa7d-435e-bec5-0aab0e04153f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "0591-3128", "generic_name": "PROGESTERONE", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROGESTERONE", "active_ingredients": [{"name": "PROGESTERONE", "strength": "50 mg/mL"}], "application_number": "NDA017362", "marketing_category": "NDA", "marketing_start_date": "19780511", "listing_expiration_date": "20261231"}