Nifedipine
- Product NDC
- 10370-677
- 11-digit product format
- 103700677
- Labeler code
- 10370
- Product ID
- 10370-677_4d6be233-5b05-4efe-88ff-370ca1be90e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA077899
- Marketing category
- ANDA
- Marketing start
- 2016-03-02
- Marketing end
- 2019-11-30
- Substance
- NIFEDIPINE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| bbd94e90-e531-9113-45c1-29860f331640 | Product name | 7 | 20230104 |
| 5e4d0a9b-8ce4-418c-bf0c-d2b4be281ffd | Product name | 4 | 20220126 |
| 308fd2ea-d88a-e021-96c1-7c2ab74d6e4b | Product name | 1 | 20140508 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 10370-677-01 | EA - Each | 10370-677 | e00cb3e7-0e61-4947-b03a-cd82599d17bd | 1 | 2016-09-02 |
| 10370-677-05 | EA - Each | 10370-677 | fd33a273-778a-4661-9ef4-be5689bfce59 | 1 | 2017-03-06 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 198034 | NIFEdipine 30 MG 24HR Extended Release Oral Tablet | PSN | 16e58a0a-b79b-46b9-ac14-9b1a0578eeab | 6 |
| 198034 | 24 HR nifedipine 30 MG Extended Release Oral Tablet | SCD | 16e58a0a-b79b-46b9-ac14-9b1a0578eeab | 6 |
| 198034 | nifedipine 30 MG 24 HR Extended Release Oral Tablet | SY | 16e58a0a-b79b-46b9-ac14-9b1a0578eeab | 6 |