Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Amgen Inc names for other drugs.
Recalls
- Jun 4, 2026 · Class II · Amgen, Inc.
Presence of Foreign Substance.
Lots: a) Lot # 1138901, Exp. Date 08/31/2026; 1149846, Exp. Date 04/30/2027 b) Lot #1138201, 1138202, 08/31/2026, 1138900, 1141143, Exp. Date 08/31/2026; 1140280, 1140281, 1142063, Exp. Date 10/31/2026; 1142062, 1142942, 1142943, Exp. Date 11/30/2026; 1144081, 1144104, Exp. Date 12/31/2026; 1146373, 114… - Jun 4, 2026 · Class II · Amgen, Inc.
Presence of Foreign Substance.
Lots: Lot #: 1138203, 1142065, Exp. Date 07/31/2026; 1145151, 1145152, 1145153, Exp. Date 2/28/2027; 1148908, 1148909, Exp. Date 05/31/2027; 1162845, 1162846, Exp. Date 11/30/2027; 1166471, 1166472, 1166473, Exp. Date 05/31/2028; 1170615, Exp. Date 08/31/2028
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ivabradine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg
- Approval
- NDA NDA206143
- On the market since
- Apr 20, 2015
- Package NDCs
55513-800-6055513-800-99- Official label
- DailyMed (National Library of Medicine), updated Nov 10, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?