NDC properties for "streptomycin (as streptomycin sulfate) 1000 MG Injection" (RxCUI 313115)
About this data
The tables show NDC propoerties for streptomycin (as streptomycin sulfate) 1000 MG Injection with the RxCUI 313115
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product
Details for streptomycin (as streptomycin sulfate) 1000 MG Injection (RxCUI 313115)
| ANDA | ANDA064210 |
|---|---|
| MMSL_CODE | BD7106 |
| MMSL_CODE | CD7106 |
| RxCUI | 313115 |
| SNOMEDCT | 324503008 |
| SPL_SET_ID | abd1f64e-4283-4370-aae8-3666316aa36e |
| VUID | 4001064 |
| Prescribable Synonym | streptomycin 1 GM Injection |
| RXNAV_STR | streptomycin 1000 MG Injection |
| RxNorm Name | streptomycin 1000 MG Injection |
| RxNorm Synonym | streptomycin (as streptomycin sulfate) 1000 MG Injection |
| RxNorm Synonym | streptomycin 1 GM Injection |
| Related queries | Interactions (for RxCUI 313115) |
NDC Properties
NDC Item 39822070601
| NDC 9 | 39822-0706 |
|---|---|
| NDC 10 | 39822-0706-1 |
| NDC Item | 39822070601 |
| Packaging | 1 in 1 VIAL |
| ANDA | ANDA064210 |
| FDA SPL set id | 725208 |
| Labeler | XGen Pharmaceuticals DJB, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1998-06-30 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 39822-0706 |
NDC Item 39822070602
| NDC 9 | 39822-0706 |
|---|---|
| NDC 10 | 39822-0706-2 |
| NDC Item | 39822070602 |
| Packaging | 10 VIAL in 1 BOX (39822-0706-2) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (39822-0706-1) |
| ANDA | ANDA064210 |
| FDA SPL set id | 725208 |
| Labeler | XGen Pharmaceuticals DJB, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1998-06-30 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 39822-0706 |
NDC Item 39822070601
| NDC 9 | 39822-0706 |
|---|---|
| NDC 10 | 39822-0706-1 |
| NDC Item | 39822070601 |
| Packaging | 1 in 1 VIAL |
| ANDA | ANDA064210 |
| FDA SPL set id | 725208 |
| Labeler | XGen Pharmaceuticals DJB, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1998-06-30 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 39822-0706 |
NDC Item 39822070602
| NDC 9 | 39822-0706 |
|---|---|
| NDC 10 | 39822-0706-2 |
| NDC Item | 39822070602 |
| Packaging | 10 VIAL in 1 BOX (39822-0706-2) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (39822-0706-1) |
| ANDA | ANDA064210 |
| FDA SPL set id | 725208 |
| Labeler | XGen Pharmaceuticals DJB, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1998-06-30 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 39822-0706 |