DEMULEN 30 (21 DAY PACK) DIN 00469327
Health Canada record
| Active ingredient(s) | ETHYNODIOL DIACETATE 2 MG; ETHINYL ESTRADIOL 30 MCG |
|---|---|
| Dosage form | Tablet |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | G03AA01 ETYNODIOL AND ESTROGEN |
| Original market date | 31-Dec-1979 |
| Current status date | 04-Jul-2019 |
| Source | Health Canada DPD |
Establishment licence of the holder
Pfizer Canada ULC — licence 100255, currently licensed, last inspection rating C (2023-08-07).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing ETHYNODIOL DIACETATE
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 00471526 | DEMULEN 30 (28 DAY PACK) | PFIZER CANADA ULC | Tablet | ETHYNODIOL DIACETATE 2 MG; ETHINYL ESTRADIOL 30 MCG | Cancelled Post Market |
| 00028630 | DEMULEN 50 (21 DAY PACK) | PFIZER CANADA ULC | Tablet | ETHYNODIOL DIACETATE 1 MG; ETHINYL ESTRADIOL 50 MCG | Cancelled Post Market |
| 00343536 | DEMULEN 50 (28 DAY PACK) | PFIZER CANADA ULC | Tablet | ETHYNODIOL DIACETATE 1 MG; ETHINYL ESTRADIOL 50 MCG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 518 | 2003-09-29 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
| 2207 | 2001-12-28 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
International API supply for ETHYNODIOL DIACETATE
1 active FDA Drug Master Files.
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