AMMONIUM CHLORIDE Drug Patent Profile
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When do Ammonium Chloride patents expire, and when can generic versions of Ammonium Chloride launch?
Ammonium Chloride is a drug marketed by Abbott, Gd Searle Llc, Mcgaw, B Braun, and Hospira. and is included in five NDAs.
The generic ingredient in AMMONIUM CHLORIDE is ammonium chloride. There are forty drug master file entries for this compound. Additional details are available on the ammonium chloride profile page.
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Questions you can ask:
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Summary for AMMONIUM CHLORIDE
US Patents: | 0 |
Applicants: | 5 |
NDAs: | 5 |
Raw Ingredient (Bulk) Api Vendors: | 53 |
Clinical Trials: | 4 |
DailyMed Link: | AMMONIUM CHLORIDE at DailyMed |
Recent Clinical Trials for AMMONIUM CHLORIDE
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Children's Mercy Hospital Kansas City | Phase 1 |
American Heart Association | Phase 1 |
University Hospitals Cleveland Medical Center | N/A |
Anatomical Therapeutic Chemical (ATC) Classes for AMMONIUM CHLORIDE
US Patents and Regulatory Information for AMMONIUM CHLORIDE
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Abbott | AMMONIUM CHLORIDE | ammonium chloride | INJECTABLE;INJECTION | 083130-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
B Braun | AMMONIUM CHLORIDE 2.14% | ammonium chloride | INJECTABLE;INJECTION | 085734-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Gd Searle Llc | AMMONIUM CHLORIDE | ammonium chloride | INJECTABLE;INJECTION | 086205-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Mcgaw | AMMONIUM CHLORIDE 0.9% IN NORMAL SALINE | ammonium chloride | INJECTABLE;INJECTION | 006580-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |