# John Wyeth & Brother Limited · 66-66 · UNITED KINGDOM — FDA import alert red lists: firms subject to detention without physical examination For John Wyeth & Brother Limited · 66-66 · UNITED KINGDOM, import alert is 66-66; import alert name is "APIs That Appear To Be Misbranded Under 502(f)(1) Because They Do Not Meet The Requirements For The Labeling Exemptions In 21 CFR 201.122"; country is UNITED KINGDOM; product is Acetazolamide; product code is 63 D - S 01 Acetazolamide (Carbonic Anhydrase Inhibitor), Active Pharm Ingred/Chems for Further Manuf; date published is 09/30/2009; address is 32 New Lane , Havant, Hampshire UNITED KINGDOM, verified against its source on 2026-09-16. - **Firm:** John Wyeth & Brother Limited _(verified: appears in the quote below)_ - **Import alert:** 66-66 - **Import alert name:** "APIs That Appear To Be Misbranded Under 502(f)(1) Because They Do Not Meet The Requirements For The Labeling Exemptions In 21 CFR 201.122" - **Country:** UNITED KINGDOM _(verified: appears in the quote below)_ - **Address:** 32 New Lane , Havant, Hampshire UNITED KINGDOM _(verified: appears in the quote below)_ - **Date published:** 09/30/2009 _(verified: appears in the quote below)_ - **Product code:** 63 D - S 01 Acetazolamide (Carbonic Anhydrase Inhibitor), Active Pharm Ingred/Chems for Further Manuf _(verified: appears in the quote below)_ - **Product:** Acetazolamide _(verified: appears in the quote below)_ - **FDA notes:** 11/2/2000 _(verified: appears in the quote below)_ ## What the source says > John Wyeth & Brother Limited Date Published : 09/30/2009 32 New Lane , Havant, Hampshire UNITED KINGDOM 63 D - S 01 Acetazolamide (Carbonic Anhydrase Inhibitor), Active Pharm Ingred/Chems for Further Manuf Date Published: 03/29/2019 Desc: Acetazolamide Notes: 11/2/2000 ## Source - https://www.accessdata.fda.gov/cms_ia/importalert_202.html Last verified: 2026-09-16. Review by: 2026-11-15. Part of [FDA import alert red lists: firms subject to detention without physical examination](https://referencesource.org/fda-import-alert-red-list/).