Details for New Drug Application (NDA): 020325
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The generic ingredient in PEPCID AC is famotidine. There are eighteen drug master file entries for this compound. One hundred and thirty-seven suppliers are listed for this compound. Additional details are available on the famotidine profile page.
Summary for 020325
| Tradename: | PEPCID AC |
| Applicant: | Kenvue Brands |
| Ingredient: | famotidine |
| Patents: | 0 |
Pharmacology for NDA: 020325
| Mechanism of Action | Histamine H2 Receptor Antagonists |
Medical Subject Heading (MeSH) Categories for 020325
Suppliers and Packaging for NDA: 020325
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| PEPCID AC | famotidine | TABLET;ORAL | 020325 | NDA | Kenvue Brands LLC | 16837-855 | 16837-855-02 | 2 POUCH in 1 CARTON (16837-855-02) / 1 TABLET, FILM COATED in 1 POUCH |
| PEPCID AC | famotidine | TABLET;ORAL | 020325 | NDA | Kenvue Brands LLC | 16837-855 | 16837-855-09 | 1 BOTTLE, PLASTIC in 1 PACKAGE (16837-855-09) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
Profile for product number 001
| Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
| Approval Date: | Apr 28, 1995 | TE: | RLD: | Yes | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 20MG | ||||
| Approval Date: | Sep 23, 2003 | TE: | RLD: | Yes | |||||
Expired US Patents for NDA 020325
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
|---|---|---|---|---|---|---|---|
| Kenvue Brands | PEPCID AC | famotidine | TABLET;ORAL | 020325-001 | Apr 28, 1995 | ⤷ Get Started Free | ⤷ Get Started Free |
| Kenvue Brands | PEPCID AC | famotidine | TABLET;ORAL | 020325-001 | Apr 28, 1995 | ⤷ Get Started Free | ⤷ Get Started Free |
| Kenvue Brands | PEPCID AC | famotidine | TABLET;ORAL | 020325-001 | Apr 28, 1995 | ⤷ Get Started Free | ⤷ Get Started Free |
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
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