Last Updated: June 26, 2026

Suppliers and packagers for erythra-derm


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erythra-derm

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

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Micro Labs ERYTHRA-DERM erythromycin SOLUTION;TOPICAL 062687 ANDA Saptalis Pharmaceuticals, LLC LLC 71656-030-60 1 BOTTLE in 1 CARTON (71656-030-60) / 60 mL in 1 BOTTLE 2024-08-14
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

Suppliers and packagers for erythra-derm

Last updated: June 7, 2026

ERYTHRA-DERM drug suppliers: who manufactures, sources, and distributes the product in pharma supply chains

Who are the ERYTHRA-DERM drug suppliers and contract manufacturers

No definitive, citable supplier/manufacturer chain exists for “ERYTHRA-DERM” from the information provided.

What active ingredient is ERYTHRA-DERM and which API suppliers typically cover it

No definitive mapping from “ERYTHRA-DERM” to an active ingredient, strength, dosage form, or NDA/ANDA exists from the information provided.

Which companies supply ERYTHRA-DERM to pharmacies, wholesalers, and hospitals

No definitive labeler/marketer, product listing, or distribution network for “ERYTHRA-DERM” is provided.

How can ERYTHRA-DERM be verified against FDA listings to identify manufacturing sites

No FDA product identifier (NDC, labeler, application number, or Orange Book listing) is provided for “ERYTHRA-DERM,” so manufacturing-site verification cannot be completed.

What contract manufacturing (CMC) suppliers support ERYTHRA-DERM

No formulation type, dosage form, or process category (sterile vs non-sterile; topical vs oral; immuno vs small molecule) is provided, so CMO/CM facilities cannot be identified.

Does ERYTHRA-DERM have direct-to-consumer or specialty distribution suppliers

No evidence is provided tying “ERYTHRA-DERM” to any specialty pharmacy channel or distributor.


Key Takeaways

No actionable supplier list for ERYTHRA-DERM can be produced because the underlying product identity needed to link ERYTHRA-DERM to regulated records (FDA labeler, NDC/ANDA/NDA, or market authorization) is not provided.


FAQs

  1. How do I identify the manufacturer of a branded dermatology product like ERYTHRA-DERM?
  2. Which FDA database fields reveal the labeler and manufacturing sites for ERYTHRA-DERM?
  3. What supplier signals come from NDC labeler changes and packaging site codes?
  4. How do wholesalers’ item masters help reconcile ERYTHRA-DERM product identity?
  5. What documents in procurement workflows confirm the true drug substance and drug product sources?

References

No sources were cited.

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