DIPHENHYDRAMINE HCI
- Product NDC
- 51662-1218
- 11-digit product format
- 516621218
- Labeler code
- 51662
- Product ID
- 51662-1218_9efa4f49-0186-e4b3-e053-2995a90a376d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DIPHENHYDRAMINE HCI
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- ANDA040140
- Marketing category
- ANDA
- Marketing start
- 2018-11-19
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 50 mg/mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1218-1 | DIPHENHYDRAMINE HCI | 1 mL in 1 CARTRIDGE | INJECTION, SOLUTION | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1218 | DIPHENHYDRAMINE HCI INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 3 | Legacy NDC, 1 package rows | 20200220_7b05c2ef-24eb-f754-e053-2991aa0afbae.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51662-1218-1 | 51662121801 | 1 mL in 1 CARTRIDGE (51662-1218-1) | 1 ml | 2018-11-19 | 0000-00-00 | No | No | Current |