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8 Hour Pain Relief

NDC 70677-1123 · STRATEGIC SOURCING SERVICES LLC

Generic nameAcetaminophen
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)ACETAMINOPHEN
Strength650 mg/1
Marketing categoryANDA

Packages

70677-1123-1 — 1 BOTTLE, PLASTIC in 1 CARTON (70677-1123-1) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70677-1004 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE, 70677-1005 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 70677-1027 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 70677-1029 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 70677-1030 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 70677-1031 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 70677-1032 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 70677-1033 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 70677-1119 — Acetaminophen, 70677-1120 — Acetaminophen, 70677-1124 — Acetaminophen, 70677-1127 — Acetaminophen, 70677-1133 — Acetaminophen, Aspirin, Caffeine, 70677-1138 — Acetaminophen, 70677-1139 — acetaminophen, 70677-1142 — Acetaminophen, 70677-1143 — Acetaminophen, 70677-1149 — Acetaminophen, Diphenhydramine HCl, 70677-1242 — ACETAMINOPHEN, 70677-1243 — Acetaminophen, +3476 more

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