Dicyclomine Hydrochloride
NDC 63323-842, Dicyclomine Hydrochloride, injection, solution, from Fresenius Kabi USA, LLC.
- Product NDC
- 63323-842
- Status
- Listed
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210257
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/63323-842 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DICYCLOMINE HYDROCHLORIDE10 mg/mL
Pharmacologic classes
Anticholinergic [EPC]; Cholinergic Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 63323-842-02 | 63323084202 | 5 VIAL, SINGLE-DOSE in 1 CARTON (63323-842-02) / 2 mL in 1 VIAL, SINGLE-DOSE (63323-842-21) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/350ce812-b9a7-401a-9793-55d2e14bb760Medicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=63323-842
Use it
Look up 63323-842 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63323-842 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63323-842. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.