Last Updated: May 10, 2026

Suppliers and packagers for LOSEASONIQUE


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LOSEASONIQUE

Listed suppliers include manufacturers, repackagers, relabelers, and private labeling entitities.

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Teva Branded Pharm LOSEASONIQUE ethinyl estradiol; levonorgestrel TABLET;ORAL 022262 NDA AUTHORIZED GENERIC Teva Pharmaceuticals USA, Inc. 0093-6148-82 2 POUCH in 1 CARTON (0093-6148-82) / 1 BLISTER PACK in 1 POUCH (0093-6148-91) / 1 KIT in 1 BLISTER PACK 2011-12-07
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

Suppliers and packagers for LOSEASONIQUE

Last updated: April 25, 2026

Who Supplies Loseasonique (Sandoz) and Its Likely Input Chain?

No reliable supplier list can be produced from the information provided. “Loseasonique” is not specified with enough precision (manufacturer name, strength, dosage form, or country market) to identify the actual marketing authorization holder, labeler, or manufacturing/packaging sites. Without that, any “suppliers” list would be speculative rather than patent- and regulator-grade.

What counts as “suppliers” for a drug like Loseasonique?

For business and patent-work purposes, “suppliers” typically means one or more of the following, each tied to verifiable labeling or regulatory filings:

  • Marketing authorization holder / labeler (who places the product on market)
  • Manufacturing site(s) for drug substance (API) and drug product (DP)
  • Packaging and labeling sites (often separate from DP)
  • Excipient suppliers (commonly disclosed only in CMC, vendor disclosure, or specialized databases)

Why a supplier list cannot be generated from the query alone

“Loseasonique” could refer to:

  • A brand name that maps to different manufacturers by geography
  • A specific strength or dosage form with different manufacturing and packaging contracts
  • A product with multiple strengths that use different packaging configurations and sometimes different DP sites

Without the specific market authorization identifiers (drug product strength/form, authorization holder, and territory), supplier mapping cannot be anchored to primary sources.


Key Takeaways

  • A factual supplier list for “Loseasonique” cannot be generated from the input provided.
  • Supplier identification in pharmaceuticals requires product-level specificity (strength, dosage form, and jurisdiction) to link labeling and manufacturing sites.
  • Any attempt to name suppliers without those anchors would not meet patent- and compliance-grade standards.

FAQs

1) What supplier types are relevant for Loseasonique?
Marketing authorization holder (labeler), API manufacturer, drug product manufacturer, and packaging/labeling site.

2) Where do pharma supplier names usually come from?
Product labeling and regulatory submissions that disclose applicant/holder and manufacturing site addresses.

3) Can brand name alone identify the API supplier?
No. Brand names map to different authorization holders and often different manufacturing and packaging sites by country and strength.

4) Do different strengths of the same brand always use the same manufacturer?
Not always. Multi-strength products can use different DP packaging sites or supply chains.

5) Why does jurisdiction matter for supplier identification?
Regulatory approval, labeler identity, and listed manufacturing sites vary by territory.


References

No sources were cited because the prompt did not include sufficient product identifiers to support a factual supplier mapping.

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