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Acetaminophen and Codeine Phosphate

NDC 13107-058 · Aurolife Pharma, LLC

Generic nameAcetaminophen and Codeine Phosphate
Dosage formTABLET
RouteORAL
Active ingredient(s)ACETAMINOPHEN, CODEINE PHOSPHATE
Strength300; 15 mg/1; mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCIII
Marketing categoryANDA

Packages

13107-058-01 — 100 TABLET in 1 BOTTLE (13107-058-01)

13107-058-05 — 500 TABLET in 1 BOTTLE (13107-058-05)

13107-058-30 — 30 TABLET in 1 BOTTLE (13107-058-30)

13107-058-99 — 1000 TABLET in 1 BOTTLE (13107-058-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11822-8003 — Acetaminophen, 11822-8791 — Diphenhydramine Hydrochloride and Acetaminophen, 11822-9440 — acetaminophen, 13107-019 — Hydrocodone Bitartrate and Acetaminophen, 13107-020 — Hydrocodone Bitartrate and Acetaminophen, 13107-021 — Hydrocodone Bitartrate and Acetaminophen, 13107-043 — Oxycodone and Acetaminophen, 13107-044 — Oxycodone and Acetaminophen, 13107-045 — Oxycodone and Acetaminophen, 13107-046 — Oxycodone and Acetaminophen, 13107-059 — Acetaminophen and Codeine Phosphate, 13107-060 — Acetaminophen and Codeine Phosphate, 13107-075 — Butalbital, Acetaminophen and Caffeine, 13107-211 — Hydrocodone Bitartrate and Acetaminophen, 13107-212 — Hydrocodone Bitartrate and Acetaminophen, 13107-213 — Hydrocodone Bitartrate and Acetaminophen, 13925-535 — butalbital, acetaminophen and caffeine, 13925-536 — butalbital, acetaminophen and caffeine, 16103-350 — Acetaminophen 500mg, 16103-353 — Acetaminophen, +3502 more

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