Promethazine Hydrochloride
- Product NDC
- 68788-7287
- 11-digit product format
- 687887287
- Labeler code
- 68788
- Product ID
- 68788-7287_58c8f2e7-48e2-4604-8dd1-a912d5a7f93d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA083426
- Marketing category
- ANDA
- Marketing start
- 2019-01-18
- Marketing end
- 0000-00-00
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68788-7287-1 | EA - Each | 68788-7287 | a104ebbf-7c04-49e8-b660-b4879956a604 | 1 | 2019-03-12 |
| 68788-7287-2 | EA - Each | 68788-7287 | 4fab3f3d-901f-4751-84b8-510c22d730e7 | 1 | 2019-03-12 |
| 68788-7287-3 | EA - Each | 68788-7287 | d73f2494-faf1-4b6b-8555-7c4832e249c9 | 1 | 2019-03-12 |
| 68788-7287-5 | EA - Each | 68788-7287 | 81c266cf-3436-4e6c-af76-82b637e803e7 | 1 | 2019-03-12 |
| 68788-7287-6 | EA - Each | 68788-7287 | 24ae7fbc-1686-415a-baf6-91ae88590ca4 | 1 | 2019-03-12 |
| 68788-7287-8 | EA - Each | 68788-7287 | 5ed149f5-cfe6-4c63-bb80-9219f6308d7f | 1 | 2019-03-12 |
| 68788-7287-9 | EA - Each | 68788-7287 | e3c7af89-7cb5-46f5-ae71-e44805981473 | 1 | 2019-03-12 |