Details for New Drug Application (NDA): 211951
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The generic ingredient in NALOXONE HYDROCHLORIDE is naloxone hydrochloride; pentazocine hydrochloride. There are twelve drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the naloxone hydrochloride; pentazocine hydrochloride profile page.
Summary for 211951
Tradename: | NALOXONE HYDROCHLORIDE |
Applicant: | Padagis Israel |
Ingredient: | naloxone hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 211951
Mechanism of Action | Opioid Antagonists |
Medical Subject Heading (MeSH) Categories for 211951
Suppliers and Packaging for NDA: 211951
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
NALOXONE HYDROCHLORIDE | naloxone hydrochloride | SPRAY, METERED;NASAL | 211951 | ANDA | Padagis Israel Pharmaceuticals Ltd | 45802-578 | 45802-578-84 | 2 VIAL, SINGLE-DOSE in 1 CARTON (45802-578-84) / .1 mL in 1 VIAL, SINGLE-DOSE (45802-578-00) |
NALOXONE HYDROCHLORIDE | naloxone hydrochloride | SPRAY, METERED;NASAL | 211951 | ANDA | Padagis Israel Pharmaceuticals Ltd | 45802-811 | 45802-811-84 | 2 VIAL, SINGLE-DOSE in 1 CARTON (45802-811-84) / .1 mL in 1 VIAL, SINGLE-DOSE (45802-811-00) |
Profile for product number 001
Active Rx/OTC/Discontinued: | OTC | Dosage: | SPRAY, METERED;NASAL | Strength | 4MG/SPRAY | ||||
Approval Date: | Jun 21, 2022 | TE: | RLD: | No |
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