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1301. Oncology pharmaceuticals: reproductive toxicity testing and labeling recommendations

1302. Considerations in demonstrating interchangeability with a reference product

1303. FDA deems certain tobacco products subject to FDA authority, sales and distribution restrictions, and health warning requirements for packages and advertisements: (revised)

1304. Extension of certain tobacco product compliance deadlines related to the final deeming rule: (revised)

1305. Interpretation of and compliance policy for certain label requirement: applicability of certain Federal Food, Drug, and Cosmetic Act requirements to vape shops

1306. Premarket tobacco product applications for electronic nicotine delivery systems

1307. Marketing clearance of diagnostic ultrasound systems and transducers: guidance for industry and Food and Drug Administration staff

1309. Compliance policy for certain compounding of oral oxitriptan (5-HTP) drug products for patients with tetrahydrobiopterin (BH4) deficiency: immediately in effect guidance for industry

1310. Delayed graft function in kidney transplantation: developing drugs for prevention