opill

Generic: norgestrel

Labeler: l. perrigo company
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name opill
Generic Name norgestrel
Labeler l. perrigo company
Dosage Form TABLET
Routes
ORAL
Active Ingredients

norgestrel .075 mg/1

Manufacturer
L. Perrigo Company

Identifiers & Regulatory

Product NDC 0113-8101
Product ID 0113-8101_fb2ad1e4-4e8a-4cee-a6e8-a823401dd8fe
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA017031
Listing Expiration 2026-12-31
Marketing Start 2024-03-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01138101
Hyphenated Format 0113-8101

Supplemental Identifiers

RxCUI
203717 762335 2676107
UNII
3J8Q1747Z2

Packaging Origin

Original Packager
true

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 opill (source: ndc)
Generic Name norgestrel (source: ndc)
Application Number NDA017031 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .075 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (0113-8101-01) / 28 TABLET in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (0113-8101-03) / 28 TABLET in 1 BLISTER PACK
  • 4 BLISTER PACK in 1 PACKAGE (0113-8101-04) / 28 TABLET in 1 BLISTER PACK
  • 6 BLISTER PACK in 1 CARTON (0113-8101-06) / 28 TABLET in 1 BLISTER PACK
source: ndc

Packages (4)

Ingredients (1)

norgestrel (.075 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fb2ad1e4-4e8a-4cee-a6e8-a823401dd8fe", "openfda": {"unii": ["3J8Q1747Z2"], "rxcui": ["203717", "762335", "2676107"], "spl_set_id": ["69dfa2ac-6a7e-4587-929c-9acabd97973b"], "manufacturer_name": ["L. Perrigo Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0113-8101-01)  / 28 TABLET in 1 BLISTER PACK", "package_ndc": "0113-8101-01", "marketing_start_date": "20240304"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0113-8101-03)  / 28 TABLET in 1 BLISTER PACK", "package_ndc": "0113-8101-03", "marketing_start_date": "20240304"}, {"sample": false, "description": "4 BLISTER PACK in 1 PACKAGE (0113-8101-04)  / 28 TABLET in 1 BLISTER PACK", "package_ndc": "0113-8101-04", "marketing_start_date": "20240322"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (0113-8101-06)  / 28 TABLET in 1 BLISTER PACK", "package_ndc": "0113-8101-06", "marketing_start_date": "20240304"}], "brand_name": "Opill", "product_id": "0113-8101_fb2ad1e4-4e8a-4cee-a6e8-a823401dd8fe", "dosage_form": "TABLET", "product_ndc": "0113-8101", "generic_name": "norgestrel", "labeler_name": "L. Perrigo Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Opill", "active_ingredients": [{"name": "NORGESTREL", "strength": ".075 mg/1"}], "application_number": "NDA017031", "marketing_category": "NDA", "marketing_start_date": "20240304", "listing_expiration_date": "20261231"}