Feverall

NDC 51672-2116 · Sun Pharmaceutical Industries, Inc.

Generic nameAcetaminophen

Dosage formSUPPOSITORY

RouteRECTAL

Active ingredient(s)ACETAMINOPHEN

Strength325 mg/1

Marketing categoryNDA

Packages

51672-2116-2 — 6 BLISTER PACK in 1 CARTON (51672-2116-2) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2116-0)

51672-2116-4 — 50 BLISTER PACK in 1 CARTON (51672-2116-4) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2116-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51467-012 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan Hydrobromide, Phenylephrine hydrochloride, 51467-013 — Acetaminophen, Phenylephrine hydrochloride, 51467-014 — Acetaminophen, Chlorpheniramine maleate, Phenylephrine hydrochloride, 51662-1273 — MEDIQUE APAP acetaminophen, 51662-1274 — MEDIQUE APAP EXTRA STRENGTH acetaminophen tablet, film coated, 51662-1540 — ACETAMINOPHEN, 51662-1665 — acetaminophen, 51662-1666 — ACETAMINOPHEN, 51672-2114 — Acetaminophen, 51672-2115 — Acetaminophen, 51672-4222 — butalbital, acetaminophen, and caffeine, 51672-4258 — Acetaminophen 250 mg and Ibuprofen 125 mg Tablets, 51672-5319 — ACETAMINOPHEN, 51824-060 — Acetaminophen, 51824-061 — Acetaminophen, 51824-069 — Acetaminophen, Diphenhydramine HCl, 51824-085 — Acetaminophen, 51824-086 — Acetaminophen, 51824-087 — Acetaminophen, 51824-099 — Acetaminophen, +3478 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.