afterplan

Generic: levonorgestrel

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name afterplan
Generic Name levonorgestrel
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levonorgestrel 1.5 mg/1

Manufacturer
SUN PHARMACEUTICAL INDUSTRIES, INC.

Identifiers & Regulatory

Product NDC 62756-723
Product ID 62756-723_f86715c5-932d-405d-b81d-286c86409b1e
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA202635
Listing Expiration 2026-12-31
Marketing Start 2017-05-12

Pharmacologic Class

Established (EPC)
progestin [epc] progestin-containing intrauterine system [epc]
Chemical Structure
progesterone congeners [cs]
Physiologic Effect
inhibit ovum fertilization [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62756723
Hyphenated Format 62756-723

Supplemental Identifiers

RxCUI
483325 2047728
UNII
5W7SIA7YZW
NUI
N0000175830 M0447349 N0000175602 N0000175832

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 afterplan (source: ndc)
Generic Name levonorgestrel (source: ndc)
Application Number ANDA202635 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (62756-723-60) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

62756-723-60 1 BLISTER PACK in 1 CARTON (62756-723-60) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

levonorgestrel (1.5 mg/1)

Linked Drug Pages (1)

AfterPlan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f86715c5-932d-405d-b81d-286c86409b1e", "openfda": {"nui": ["N0000175830", "M0447349", "N0000175602", "N0000175832"], "unii": ["5W7SIA7YZW"], "rxcui": ["483325", "2047728"], "spl_set_id": ["c30c7bc2-04fa-4590-96f5-5bcf4bba3f1a"], "pharm_class_cs": ["Progesterone Congeners [CS]"], "pharm_class_pe": ["Inhibit Ovum Fertilization [PE]"], "pharm_class_epc": ["Progestin [EPC]", "Progestin-containing Intrauterine System [EPC]"], "manufacturer_name": ["SUN PHARMACEUTICAL INDUSTRIES, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (62756-723-60)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "62756-723-60", "marketing_start_date": "20170512"}], "brand_name": "AfterPlan", "product_id": "62756-723_f86715c5-932d-405d-b81d-286c86409b1e", "dosage_form": "TABLET", "pharm_class": ["Inhibit Ovum Fertilization [PE]", "Progesterone Congeners [CS]", "Progesterone Congeners [CS]", "Progestin [EPC]", "Progestin-containing Intrauterine Device [EPC]"], "product_ndc": "62756-723", "generic_name": "levonorgestrel", "labeler_name": "SUN PHARMACEUTICAL INDUSTRIES, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AfterPlan", "active_ingredients": [{"name": "LEVONORGESTREL", "strength": "1.5 mg/1"}], "application_number": "ANDA202635", "marketing_category": "ANDA", "marketing_start_date": "20170512", "listing_expiration_date": "20261231"}