|
|
------------------------------------------------------------------------Contents (.PDF) Federal RegisterContents (.TXT) Vol. 64, No.38Friday, February 26, 1999------------------------------------------------------------------------NADA 141-063, CVM98161. Implantation or Injectable Dosage Form New Animal Drugs; Florfenicol Solution. Page 9435 [FR Doc. 99-4762] [TXT] [PDF]RULES Docket No. 93N-0371, OC9945. Agency Information Collection Activities; Announcement of OMB Approval; Prescription Drug Product Labeling, Medication Guide Requirements. Page 9515 [FR Doc. 99-4765] [TXT] [PDF]Freedom of Information SummaryNOTICES Docket No. 97N-0165, OC9938. Agency Information Collection Activities; Announcement of OMB Approval; Regulations Requiring Manufacturers to Assess the Safety and Effectiveness of New Drugs and Biological Products in Pediatric Patients. Page 9515 [FR Doc. 99-4766] [TXT] [PDF]Supporting Statement DOCKET No. 84N-0102, OC998. Cumulative List of Orphan Drug and Biological Designations. Pages 9515-9516 [FR Doc. 99-4764] [TXT] [PDF]Supporting Statement Docket No. 95D-0349, CDER992. Guidance for Industry on SUPAC09IR/MR: Immediate Release and Modified Release Solid Oral Dosage Forms, Manufacturing Equipment Addendum; Availability. Page 9516 [FR Doc. 99-4767] [TXT] [PDF] Docket No. 99D-0236, CDER98198. Draft Guidance for Industry on Skin Irritation and Sensitization Testing of Generic Transdermal Drug Products; Availability. Page 9516-9517 [FR Doc. 99-4763] [TXT] [PDF] Written comments by April 27, 1999Guidance Draft Guidance |