Glycopyrrolate
- Product NDC
- 0641-6033
- 11-digit product format
- 006416033
- Labeler code
- 0641
- Product ID
- 0641-6033_d2cb6514-ba29-4b95-b9a1-6cd21a5e2371
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glycopyrrolate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- West-ward Pharmaceutical Corp.
- Application
- NDA017558
- Marketing category
- NDA
- Marketing start
- 1975-02-06
- Marketing end
- 0000-00-00
- Substance
- GLYCOPYRROLATE
- Active strength
- 0 mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0641-6033 | GLYCOPYRROLATE INJECTION [WEST-WARD PHARMACEUTICAL CORP.] | 3 | Legacy NDC | 20120612_61767a0d-c94c-44d8-b35c-316a5731a275.zip |