progesterone
Generic: progesterone
Labeler: dr. reddys laboratories, inc.Drug Facts
Product Profile
Brand Name
progesterone
Generic Name
progesterone
Labeler
dr. reddys laboratories, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
progesterone 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43598-350
Product ID
43598-350_4b8f3d16-f096-32f0-65f9-230ab8c292b7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208801
Listing Expiration
2026-12-31
Marketing Start
2017-03-25
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43598350
Hyphenated Format
43598-350
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
ANDA208801 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (43598-350-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b8f3d16-f096-32f0-65f9-230ab8c292b7", "openfda": {"nui": ["M0017672", "N0000175601"], "unii": ["4G7DS2Q64Y"], "rxcui": ["260243", "312641"], "spl_set_id": ["efded380-02ff-68c9-13e4-47a561ede440"], "pharm_class_cs": ["Progesterone [CS]"], "pharm_class_epc": ["Progesterone [EPC]"], "manufacturer_name": ["Dr. Reddys Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (43598-350-01)", "package_ndc": "43598-350-01", "marketing_start_date": "20170325"}], "brand_name": "Progesterone", "product_id": "43598-350_4b8f3d16-f096-32f0-65f9-230ab8c292b7", "dosage_form": "CAPSULE", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "43598-350", "generic_name": "Progesterone", "labeler_name": "Dr. Reddys Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Progesterone", "active_ingredients": [{"name": "PROGESTERONE", "strength": "200 mg/1"}], "application_number": "ANDA208801", "marketing_category": "ANDA", "marketing_start_date": "20170325", "listing_expiration_date": "20261231"}