Class I · High risk
Tydemy
Failed Stability Specification and Failed Impurities/Degradation Specifications: out of specification for inactive content ascorbic acid and MTHFRC-7impurity test
National Drug Code
Is NDC 68180-0904-73 recalled?
Tydemy · 3 POUCH in 1 CARTON (68180-904-73) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK * 21 TABLET, FILM COATED in 1 BLISTER PACK (68180-905-74) * 7 TABLET, FILM COATED in 1 BLISTER PACK (68180-
Yes — this exact package was recalled
1 FDA recall names the code 68180-0904-73 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Drospirenone, Ethinyl Estradiol and Levomefolate Calcium and Levomefolate Calcium
- Form
- Kit
- Labeler
- Lupin Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 68180-0904
Recalls naming this package
Class III · Low risk
Tydemy
Subpotent Drug
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 68180-0723 Cefdinir 7
- 68180-0405 Cefixime 4
- 68180-0519 Lisinopril and Hydrochlorothiazide 4
- 68180-0422 Moxifloxacin 3
- 68180-0435 See recall 3
- 68180-0633 See recall 3
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.